Chimeric Polypeptides Having Cellulolytic Enhancing Activity and Polynucleotides Encoding Same

ABSTRACT

The present invention relates to chimeric GH61 polypeptides having cellulolytic enhancing activity. The present invention also relates to polynucleotides encoding the chimeric GH61 polypeptides; nucleic acid constructs, vectors, and host cells comprising the polynucleotides; and methods of using the chimeric GH61 polypeptides.

CROSS-REFERENCE TO A RELATED APPLICATION

This application claims the benefit of U.S. Provisional Application Ser. No. 61/415,066 filed Nov. 18, 2010, which is incorporated herein by reference.

STATEMENT AS TO RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSORED RESEARCH AND DEVELOPMENT

This invention was made with Government support under Cooperative Agreement DE-FC36-08GO18080 awarded by the Department of Energy. The government has certain rights in this invention.

REFERENCE TO A SEQUENCE LISTING

This application contains a Sequence Listing in computer readable form, which is incorporated herein by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to chimeric GH61 polypeptides having cellulolytic enhancing activity, polynucleotides encoding the chimeric GH61 polypeptides, methods of producing the chimeric GH61 polypeptides, and methods of using the chimeric GH61 polypeptides.

2. Description of the Related Art

Cellulose is a polymer of the simple sugar glucose covalently linked by beta-1,4-bonds. Many microorganisms produce enzymes that hydrolyze beta-linked glucans. These enzymes include endoglucanases, cellobiohydrolases, and beta-glucosidases. Endoglucanases digest the cellulose polymer at random locations, opening it to attack by cellobiohydrolases. Cellobiohydrolases sequentially release molecules of cellobiose from the ends of the cellulose polymer. Cellobiose is a water-soluble beta-1,4-linked dimer of glucose. Beta-glucosidases hydrolyze cellobiose to glucose.

The conversion of lignocellulosic feedstocks into ethanol has the advantages of the ready availability of large amounts of feedstock, the desirability of avoiding burning or land filling the materials, and the cleanliness of the ethanol fuel. Wood, agricultural residues, herbaceous crops, and municipal solid wastes have been considered as feedstocks for ethanol production. These materials primarily consist of cellulose, hemicellulose, and lignin. Once the lignocellulose is converted to fermentable sugars, e.g., glucose, the fermentable sugars are easily fermented by yeast into ethanol.

WO 2005/074647, WO 2008/148131, and WO 2011/035027 disclose isolated GH61 polypeptides having cellulolytic enhancing activity and the polynucleotides thereof from Thielavia terrestris. WO 2005/074656 and WO 2010/065830 disclose isolated GH61 polypeptides having cellulolytic enhancing activity and the polynucleotides thereof from Thermoascus aurantiacus. WO 2007/089290 discloses an isolated GH61 polypeptide having cellulolytic enhancing activity and the polynucleotide thereof from Trichoderma reesei. WO 2009/085935, WO 2009/085859, WO 2009/085864, and WO 2009/085868 disclose isolated GH61 polypeptides having cellulolytic enhancing activity and the polynucleotides thereof from Myceliophthora thermophila. WO 2010/138754 discloses isolated GH61 polypeptides having cellulolytic enhancing activity and the polynucleotides thereof from Aspergillus fumigatus. WO 2011/005867 discloses isolated GH61 polypeptides having cellulolytic enhancing activity and the polynucleotides thereof from Penicillium pinophilum. WO 2011/039319 discloses isolated GH61 polypeptides having cellulolytic enhancing activity and the polynucleotides thereof from Thermoascus sp. WO 2011/041397 discloses isolated GH61 polypeptides having cellulolytic enhancing activity and the polynucleotides thereof from Penicillium sp. WO 2011/041504 discloses isolated GH61 polypeptides having cellulolytic enhancing activity and the polynucleotides thereof from Thermoascus crustaceous. WO 2008/151043 discloses methods of increasing the activity of a GH61 polypeptide having cellulolytic enhancing activity by adding a soluble activating divalent metal cation to a composition comprising the polypeptide.

It would be advantageous in the art to improve the ability of polypeptides having cellulolytic enhancing activity to enhance enzymatic degradation of lignocellulosic feedstocks.

The present invention provides chimeric GH61 polypeptides having cellulolytic enhancing activity with improved properties.

SUMMARY OF THE INVENTION

The present invention relates to isolated chimeric GH61 polypeptides having cellulolytic enhancing activity, comprising:

(a) a first GH61 polypeptide fragment at the N-terminal end of the chimeric GH61 polypeptide selected from the group consisting of (i) a polypeptide fragment having at least 60% sequence identity to amino acids 22 to 84 of SEQ ID NO: 78; (ii) a polypeptide fragment encoded by a polynucleotide that hybridizes under at least low stringency conditions with nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polypeptide fragment encoded by a polynucleotide having at least 60% sequence identity to nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof; and (iv) a polypeptide fragment comprising or consisting of amino acids 22 to 84 of SEQ ID NO: 78;

(b) a second GH61 polypeptide fragment at the C-terminal end of the first polypeptide fragment selected from the group consisting of (i) a polypeptide fragment having at least 60% sequence identity to amino acids 85 to 207 of SEQ ID NO: 94; (ii) a polypeptide fragment encoded by a polynucleotide that hybridizes under at least low stringency conditions with nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polypeptide fragment encoded by a polynucleotide having at least 60% sequence identity to nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof; and (iv) a polypeptide fragment comprising or consisting of amino acids 85 to 207 of SEQ ID NO: 94; and

(c) a third GH61 polypeptide fragment at the C-terminal end of the second polypeptide fragment selected from the group consisting of (i) a polypeptide fragment having at least 60% sequence identity to amino acids 208 to 249 of SEQ ID NO: 78; (ii) a polypeptide fragment encoded by a polynucleotide that hybridizes under at least low stringency conditions with nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polypeptide fragment encoded by a polynucleotide having at least 60% sequence identity to nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof; and (iv) a polypeptide fragment comprising or consisting of amino acids 208 to 249 of SEQ ID NO: 78.

The present invention also relates to isolated polynucleotides encoding the chimeric GH61 polypeptides; nucleic acid constructs, vectors, and host cells comprising the polynucleotides; and methods of producing the chimeric GH61 polypeptides.

The present invention also relates to methods for degrading or converting a cellulosic material, comprising: treating the cellulosic material with an enzyme composition in the presence of such a chimeric GH61 polypeptide having cellulolytic enhancing activity.

The present invention also relates to methods for producing a fermentation product, comprising:

(a) saccharifying a cellulosic material with an enzyme composition in the presence of such a chimeric GH61 polypeptide having cellulolytic enhancing activity;

(b) fermenting the saccharified cellulosic material with one or more (e.g., several) fermenting microorganisms to produce the fermentation product; and

(c) recovering the fermentation product from the fermentation.

The present invention also relates to methods of fermenting a cellulosic material, comprising: fermenting the cellulosic material with one or more (e.g., several) fermenting microorganisms, wherein the cellulosic material is saccharified with an enzyme composition in the presence of such a chimeric GH61 polypeptide having cellulolytic enhancing activity.

The present invention also relates to detergent compositions comprising such a chimeric GH61 polypeptide and a surfactant.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 shows the effect of the addition of an Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A chimeric polypeptide on conversion of phosphoric acid swollen cellulose (PASC) by Aspergillus fumigatus beta-glucosidase.

FIGS. 2A and 2B shows determinations of Td (denaturation temperature) of an Aspergillus fumigatus wild-type GH61B polypeptide and the Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A chimeric polypeptide, respectively, by differential scanning calorimetry.

DEFINITIONS

Acetylxylan Esterase: The term “acetylxylan esterase” means a carboxylesterase (EC 3.1.1.72) that catalyzes the hydrolysis of acetyl groups from polymeric xylan, acetylated xylose, acetylated glucose, alpha-napthyl acetate, and p-nitrophenyl acetate. For purposes of the present invention, acetylxylan esterase activity is determined using 0.5 mM p-nitrophenylacetate as substrate in 50 mM sodium acetate pH 5.0 containing 0.01% TWEEN™ 20 (polyoxyethylene sorbitan monolaurate). One unit of acetylxylan esterase is defined as the amount of enzyme capable of releasing 1 μmole of p-nitrophenolate anion per minute at pH 5, 25° C.

Allelic variant: The term “allelic variant” means any of two or more alternative forms of a gene occupying the same chromosomal locus. Allelic variation arises naturally through mutation, and may result in polymorphism within populations. Gene mutations can be silent (no change in the encoded polypeptide) or may encode polypeptides having altered amino acid sequences. An allelic variant of a polypeptide is a polypeptide encoded by an allelic variant of a gene.

Alpha-L-arabinofuranosidase: The term “alpha-L-arabinofuranosidase” means an alpha-L-arabinofuranoside arabinofuranohydrolase (EC 3.2.1.55) that catalyzes the hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans, and arabinogalactans. Alpha-L-arabinofuranosidase is also known as arabinosidase, alpha-arabinosidase, alpha-L-arabinosidase, alpha-arabinofuranosidase, polysaccharide alpha-L-arabinofuranosidase, alpha-L-arabinofuranoside hydrolase, L-arabinosidase, or alpha-L-arabinanase. For purposes of the present invention, alpha-L-arabinofuranosidase activity is determined using 5 mg of medium viscosity wheat arabinoxylan (Megazyme International Ireland, Ltd., Bray, Co. Wicklow, Ireland) per ml of 100 mM sodium acetate pH 5 in a total volume of 200 μl for 30 minutes at 40° C. followed by arabinose analysis by AMINEX® HPX-87H column chromatography (Bio-Rad Laboratories, Inc., Hercules, Calif., USA).

Alpha-glucuronidase: The term “alpha-glucuronidase” means an alpha-D-glucosiduronate glucuronohydrolase (EC 3.2.1.139) that catalyzes the hydrolysis of an alpha-D-glucuronoside to D-glucuronate and an alcohol. For purposes of the present invention, alpha-glucuronidase activity is determined according to de Vries, 1998, J. Bacteriol. 180: 243-249. One unit of alpha-glucuronidase equals the amount of enzyme capable of releasing 1 μmole of glucuronic or 4-O-methylglucuronic acid per minute at pH 5, 40° C.

Beta-glucosidase: The term “beta-glucosidase” means a beta-D-glucoside glucohydrolase (E.C. 3.2.1.21) that catalyzes the hydrolysis of terminal non-reducing beta-D-glucose residues with the release of beta-D-glucose. For purposes of the present invention, beta-glucosidase activity is determined using p-nitrophenyl-beta-D-glucopyranoside as substrate according to the procedure of Venturi et al., 2002, Extracellular beta-D-glucosidase from Chaetomium thermophilum var. coprophilum: production, purification and some biochemical properties, J. Basic Microbiol. 42: 55-66. One unit of beta-glucosidase is defined as 1.0 μmole of p-nitrophenolate anion produced per minute at 25° C., pH 4.8 from 1 mM p-nitrophenyl-beta-D-glucopyranoside as substrate in 50 mM sodium citrate containing 0.01% TWEEN® 20.

Beta-xylosidase: The term “beta-xylosidase” means a beta-D-xyloside xylohydrolase (E.C. 3.2.1.37) that catalyzes the exo-hydrolysis of short beta-(4)-xylooligosaccharides to remove successive D-xylose residues from non-reducing termini. For purposes of the present invention, one unit of beta-xylosidase is defined as 1.0 μmole of p-nitrophenolate anion produced per minute at 40° C., pH 5 from 1 mM p-nitrophenyl-beta-D-xyloside as substrate in 100 mM sodium citrate containing 0.01% TWEEN® 20.

cDNA: The term “cDNA” means a DNA molecule that can be prepared by reverse transcription from a mature, spliced, mRNA molecule obtained from a eukaryotic or prokaryotic cell. cDNA lacks intron sequences that may be present in the corresponding genomic DNA. The initial, primary RNA transcript is a precursor to mRNA that is processed through a series of steps, including splicing, before appearing as mature spliced mRNA.

Cellobiohydrolase: The term “cellobiohydrolase” means a 1,4-beta-D-glucan cellobiohydrolase (E.C. 3.2.1.91 and E.C. 3.2.1.176) that catalyzes the hydrolysis of 1,4-beta-D-glucosidic linkages in cellulose, cellooligosaccharides, or any beta-1,4-linked glucose containing polymer, releasing cellobiose from the reducing or non-reducing ends of the chain (Teeri, 1997, Crystalline cellulose degradation: New insight into the function of cellobiohydrolases, Trends in Biotechnology 15: 160-167; Teeri et al., 1998, Trichoderma reesei cellobiohydrolases: why so efficient on crystalline cellulose?, Biochem. Soc. Trans. 26: 173-178). Cellobiohydrolase activity is determined according to the procedures described by Lever et al., 1972, Anal. Biochem. 47: 273-279; van Tilbeurgh et al., 1982, FEBS Letters, 149: 152-156; van Tilbeurgh and Claeyssens, 1985, FEBS Letters, 187: 283-288; and Tomme et al., 1988, Eur. J. Biochem. 170: 575-581. In the present invention, the Tomme et al. method can be used to determine cellobiohydrolase activity.

Cellulolytic enzyme or cellulase: The term “cellulolytic enzyme” or “cellulase” means one or more (e.g., several) enzymes that hydrolyze a cellulosic material. Such enzymes include endoglucanase(s), cellobiohydrolase(s), beta-glucosidase(s), or combinations thereof. The two basic approaches for measuring cellulolytic activity include: (1) measuring the total cellulolytic activity, and (2) measuring the individual cellulolytic activities (endoglucanases, cellobiohydrolases, and beta-glucosidases) as reviewed in Zhang et al., Outlook for cellulase improvement: Screening and selection strategies, 2006, Biotechnology Advances 24: 452-481. Total cellulolytic activity is usually measured using insoluble substrates, including Whatman No 1 filter paper, microcrystalline cellulose, bacterial cellulose, algal cellulose, cotton, pretreated lignocellulose, etc. The most common total cellulolytic activity assay is the filter paper assay using Whatman No 1 filter paper as the substrate. The assay was established by the International Union of Pure and Applied Chemistry (IUPAC) (Ghose, 1987, Measurement of cellulase activities, Pure Appl. Chem. 59: 257-68).

For purposes of the present invention, cellulolytic enzyme activity is determined by measuring the increase in hydrolysis of a cellulosic material by cellulolytic enzyme(s) under the following conditions: 1-50 mg of cellulolytic enzyme protein/g of cellulose in PCS (or other pretreated cellulosic material) for 3-7 days at a suitable temperature, e.g., 50° C., 55° C., or 60° C., compared to a control hydrolysis without addition of cellulolytic enzyme protein. Typical conditions are 1 ml reactions, washed or unwashed PCS, 5% insoluble solids, 50 mM sodium acetate pH 5, 1 mM MnSO₄, 50° C., 55° C., or 60° C., 72 hours, sugar analysis by AMINEX® HPX-87H column (Bio-Rad Laboratories, Inc., Hercules, Calif., USA).

Cellulosic material: The term “cellulosic material” means any material containing cellulose. The predominant polysaccharide in the primary cell wall of biomass is cellulose, the second most abundant is hemicellulose, and the third is pectin. The secondary cell wall, produced after the cell has stopped growing, also contains polysaccharides and is strengthened by polymeric lignin covalently cross-linked to hemicellulose. Cellulose is a homopolymer of anhydrocellobiose and thus a linear beta-(1-4)-D-glucan, while hemicelluloses include a variety of compounds, such as xylans, xyloglucans, arabinoxylans, and mannans in complex branched structures with a spectrum of substituents. Although generally polymorphous, cellulose is found in plant tissue primarily as an insoluble crystalline matrix of parallel glucan chains. Hemicelluloses usually hydrogen bond to cellulose, as well as to other hemicelluloses, which help stabilize the cell wall matrix.

Cellulose is generally found, for example, in the stems, leaves, hulls, husks, and cobs of plants or leaves, branches, and wood of trees. The cellulosic material can be, but is not limited to, agricultural residue, herbaceous material (including energy crops), municipal solid waste, pulp and paper mill residue, waste paper, and wood (including forestry residue) (see, for example, Wiselogel et al., 1995, in Handbook on Bioethanol (Charles E. Wyman, editor), pp. 105-118, Taylor & Francis, Washington D.C.; Wyman, 1994, Bioresource Technology 50: 3-16; Lynd, 1990, Applied Biochemistry and Biotechnology 24/25: 695-719; Mosier et al., 1999, Recent Progress in Bioconversion of Lignocellulosics, in Advances in Biochemical Engineering/Biotechnology, T. Scheper, managing editor, Volume 65, pp. 23-40, Springer-Verlag, New York). It is understood herein that the cellulose may be in the form of lignocellulose, a plant cell wall material containing lignin, cellulose, and hemicellulose in a mixed matrix. In a preferred aspect, the cellulosic material is any biomass material. In another preferred aspect, the cellulosic material is lignocellulose, which comprises cellulose, hemicelluloses, and lignin.

In one aspect, the cellulosic material is agricultural residue. In another aspect, the cellulosic material is herbaceous material (including energy crops). In another aspect, the cellulosic material is municipal solid waste. In another aspect, the cellulosic material is pulp and paper mill residue. In another aspect, the cellulosic material is waste paper. In another aspect, the cellulosic material is wood (including forestry residue).

In another aspect, the cellulosic material is arundo. In another aspect, the cellulosic material is bagasse. In another aspect, the cellulosic material is bamboo. In another aspect, the cellulosic material is corn cob. In another aspect, the cellulosic material is corn fiber. In another aspect, the cellulosic material is corn stover. In another aspect, the cellulosic material is miscanthus. In another aspect, the cellulosic material is orange peel. In another aspect, the cellulosic material is rice straw. In another aspect, the cellulosic material is switchgrass. In another aspect, the cellulosic material is wheat straw.

In another aspect, the cellulosic material is aspen. In another aspect, the cellulosic material is eucalyptus. In another aspect, the cellulosic material is fir. In another aspect, the cellulosic material is pine. In another aspect, the cellulosic material is poplar. In another aspect, the cellulosic material is spruce. In another aspect, the cellulosic material is willow.

In another aspect, the cellulosic material is algal cellulose. In another aspect, the cellulosic material is bacterial cellulose. In another aspect, the cellulosic material is cotton linter. In another aspect, the cellulosic material is filter paper. In another aspect, the cellulosic material is microcrystalline cellulose. In another aspect, the cellulosic material is phosphoric-acid treated cellulose.

In another aspect, the cellulosic material is an aquatic biomass. As used herein the term “aquatic biomass” means biomass produced in an aquatic environment by a photosynthesis process. The aquatic biomass can be algae, emergent plants, floating-leaf plants, or submerged plants.

The cellulosic material may be used as is or may be subjected to pretreatment, using conventional methods known in the art, as described herein. In a preferred aspect, the cellulosic material is pretreated.

Chimeric GH61 polypeptide: The term “chimeric GH61 polypeptide” means a polypeptide whose composition is generated by replacing a sequence of amino acids from one parent GH61 polypeptide with those from homologous positions of one or more (e.g., several) other parent GH61 polypeptides.

The chimeric GH61 polypeptides of the present invention have at least 20%, e.g., at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, and at least 100% of the cellulolytic enhancing activity of the mature polypeptide of SEQ ID NO: 144.

The chimeric GH61 polypeptides having cellulolytic enhancing activity enhance the hydrolysis of a cellulosic material catalyzed by enzyme having cellulolytic activity by reducing the amount of cellulolytic enzyme required to reach the same degree of hydrolysis preferably at least 1.01-fold, e.g., at least 1.05-fold, at least 1.10-fold, at least 1.25-fold, at least 1.5-fold, at least 2-fold, at least 3-fold, at least 4-fold, at least 5-fold, at least 10-fold, or at least 20-fold.

Coding sequence: The term “coding sequence” means a polynucleotide, which directly specifies the amino acid sequence of a polypeptide. The boundaries of the coding sequence are generally determined by an open reading frame, which begins with a start codon such as ATG, GTG, or TTG and ends with a stop codon such as TAA, TAG, or TGA. The coding sequence may be a genomic DNA, cDNA, synthetic DNA, or a combination thereof.

Control sequences: The term “control sequences” means nucleic acid sequences necessary for expression of a polynucleotide encoding a chimeric GH61 polypeptide of the present invention. Each control sequence may be native (i.e., from the same gene) or foreign (i.e., from a different gene) to the polynucleotide encoding the polypeptide or native or foreign to each other. Such control sequences include, but are not limited to, a leader, polyadenylation sequence, propeptide sequence, promoter, signal peptide sequence, and transcription terminator. At a minimum, the control sequences include a promoter, and transcriptional and translational stop signals. The control sequences may be provided with linkers for the purpose of introducing specific restriction sites facilitating ligation of the control sequences with the coding region of the polynucleotide encoding a polypeptide.

Endoglucanase: The term “endoglucanase” means an endo-1,4-(1,3;1,4)-beta-D-glucan 4-glucanohydrolase (E.C. 3.2.1.4) that catalyzes endohydrolysis of 1,4-beta-D-glycosidic linkages in cellulose, cellulose derivatives (such as carboxymethyl cellulose and hydroxyethyl cellulose), lichenin, beta-1,4 bonds in mixed beta-1,3 glucans such as cereal beta-D-glucans or xyloglucans, and other plant material containing cellulosic components. Endoglucanase activity can be determined by measuring reduction in substrate viscosity or increase in reducing ends determined by a reducing sugar assay (Zhang et al., 2006, Biotechnology Advances 24: 452-481). For purposes of the present invention, endoglucanase activity is determined using carboxymethyl cellulose (CMC) as substrate according to the procedure of Ghose, 1987, Pure and Appl. Chem. 59: 257-268, at pH 5, 40° C.

Expression: The term “expression” includes any step involved in the production of a polypeptide including, but not limited to, transcription, post-transcriptional modification, translation, post-translational modification, and secretion.

Expression vector: The term “expression vector” means a linear or circular DNA molecule that comprises a polynucleotide encoding a polypeptide and is operably linked to control sequences that provide for its expression.

Family 61 glycoside hydrolase: The term “Family 61 glycoside hydrolase” or “Family GH61” or “GH61” means a polypeptide falling into the glycoside hydrolase Family 61 according to Henrissat B., 1991, A classification of glycosyl hydrolases based on amino-acid sequence similarities, Biochem. J. 280: 309-316, and Henrissat B., and Bairoch A., 1996, Updating the sequence-based classification of glycosyl hydrolases, Biochem. J. 316: 695-696. The enzymes in this family were originally classified as a glycoside hydrolase family based on measurement of very weak endo-1,4-beta-D-glucanase activity in one family member. The structure and mode of action of these enzymes are non-canonical and they cannot be considered as bona fide glycosidases. However, they are kept in the CAZy classification on the basis of their capacity to enhance the breakdown of lignocellulose when used in conjunction with a cellulase or a mixture of cellulases.

Feruloyl esterase: The term “feruloyl esterase” means a 4-hydroxy-3-methoxycinnamoyl-sugar hydrolase (EC 3.1.1.73) that catalyzes the hydrolysis of 4-hydroxy-3-methoxycinnamoyl (feruloyl) groups from esterified sugar, which is usually arabinose in natural biomass substrates, to produce ferulate (4-hydroxy-3-methoxycinnamate). Feruloyl esterase is also known as ferulic acid esterase, hydroxycinnamoyl esterase, FAE-III, cinnamoyl ester hydrolase, FAEA, cinnAE, FAE-I, or FAE-II. For purposes of the present invention, feruloyl esterase activity is determined using 0.5 mM p-nitrophenylferulate as substrate in 50 mM sodium acetate pH 5.0. One unit of feruloyl esterase equals the amount of enzyme capable of releasing 1 μmole of p-nitrophenolate anion per minute at pH 5, 25° C.

Fragment: The term “fragment” means a polypeptide having one or more (e.g., several) amino acids deleted from the amino and/or carboxyl terminus of a mature polypeptide; wherein the fragment has biological activity.

Hemicellulolytic enzyme or hemicellulase: The term “hemicellulolytic enzyme” or “hemicellulase” means one or more (e.g., several) enzymes that hydrolyze a hemicellulosic material. See, for example, Shallom, D. and Shoham, Y. Microbial hemicellulases. Current Opinion In Microbiology, 2003, 6(3): 219-228). Hemicellulases are key components in the degradation of plant biomass. Examples of hemicellulases include, but are not limited to, an acetylmannan esterase, an acetylxylan esterase, an arabinanase, an arabinofuranosidase, a coumaric acid esterase, a feruloyl esterase, a galactosidase, a glucuronidase, a glucuronoyl esterase, a mannanase, a mannosidase, a xylanase, and a xylosidase. The substrates of these enzymes, the hemicelluloses, are a heterogeneous group of branched and linear polysaccharides that are bound via hydrogen bonds to the cellulose microfibrils in the plant cell wall, crosslinking them into a robust network. Hemicelluloses are also covalently attached to lignin, forming together with cellulose a highly complex structure. The variable structure and organization of hemicelluloses require the concerted action of many enzymes for its complete degradation. The catalytic modules of hemicellulases are either glycoside hydrolases (GHs) that hydrolyze glycosidic bonds, or carbohydrate esterases (CEs), which hydrolyze ester linkages of acetate or ferulic acid side groups. These catalytic modules, based on homology of their primary sequence, can be assigned into GH and CE families. Some families, with an overall similar fold, can be further grouped into clans, marked alphabetically (e.g., GH-A). A most informative and updated classification of these and other carbohydrate active enzymes is available in the Carbohydrate-Active Enzymes (CAZy) database. Hemicellulolytic enzyme activities can be measured according to Ghose and Bisaria, 1987, Pure & Appl. Chem. 59: 1739-1752, at a suitable temperature, e.g., 50° C., 55° C., or 60° C., and pH, e.g., 5.0 or 5.5.

High stringency conditions: The term “high stringency conditions” means for probes of at least 100 nucleotides in length, prehybridization and hybridization at 42° C. in 5×SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 50% formamide, following standard Southern blotting procedures for 12 to 24 hours. The carrier material is finally washed three times each for 15 minutes using 2×SSC, 0.2% SDS at 65° C.

Host cell: The term “host cell” means any cell type that is susceptible to transformation, transfection, transduction, or the like with a nucleic acid construct or expression vector comprising a polynucleotide of the present invention. The term “host cell” encompasses any progeny of a parent cell that is not identical to the parent cell due to mutations that occur during replication.

Increased thermal activity: The term “increased thermal activity” means a higher or broader temperature-dependent activity profile of a chimeric GH61 polypeptide compared to the temperature-dependent activity profile of a parent GH61 polypeptide thereof. The increased thermal activity of the chimeric GH61 polypeptide enhances catalysis of a reaction at one or more (e.g., several) specific temperatures relative to a parent GH61 polypeptide thereof. A more thermoactive chimeric GH61 polypeptide will lead to a decrease in the time required and/or a decrease in the enzyme concentration required for catalysis of the reaction. The increased thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof can be assessed, for example, under conditions of one or more (e.g., several) temperatures. For example, the one or more (e.g., several) temperatures can be any temperature or temperature in the range of 25° C. to 95° C., e.g., 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, or 95° C. (or in between) at one or more (e.g., several) pHs in the range of 3 to 9, e.g., 3.0, 3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 6.5, 7.0, 7.5, 8.0, 8.5, or 9.0 (or in between). In one aspect, the increase in thermal activity is determined over a range of temperatures selected from temperatures between 25° C. and 95° C.

The increased thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof can be determined using any enzyme assay known in the art for GH61 polypeptides having cellulolytic enhancing activity. See for example, WO 2005/074647, WO 2008/148131 WO 2005/074656, WO 2010/065830, WO 2007/089290, WO 2009/085935, WO 2009/085859, WO 2009/085864, WO 2009/085868, and WO 2008/151043, which are incorporated herein by reference. Alternatively, the increased thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof can be determined using any application assay for the chimeric GH61 polypeptide where the performance of the chimeric GH61 polypeptide is compared to the a parent GH61 polypeptide. For example, the application assay described in Example 8 can be used.

One or more (e.g., several) of the parent GH61 polypeptides in which fragments thereof are combined to produce a chimeric GH61 polypeptide may be used to determine the increase in thermal activity of the chimeric GH61 polypeptide.

A chimeric GH61 polypeptide with increased thermal activity may or may not display increased thermostability relative to a parent GH61 polypeptide thereof. For example, a chimeric GH61 polypeptide may have an increased thermal activity relative to a parent GH61 polypeptide thereof, but does not have increased thermostability.

Increased thermostability: The term “increased thermostability” means a higher retention of cellulolytic enhancing activity of a chimeric GH61 polypeptide after a period of incubation at a temperature relative to a parent GH61 polypeptide thereof. The increased thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof can be assessed, for example, under conditions of one or more (e.g., several) temperatures. For example, the one or more (e.g., several) temperatures can be any temperature or temperatures in the range of 45° C. to 95° C., e.g., 45, 50, 55, 60, 65, 70, 75, 80, 85, or 95° C. (or in between) at one or more (e.g., several) pHs in the range of 3 to 9, e.g., 3.0, 3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 6.5, 7.0, 7.5, 8.0, 8.5, or 9.0 (or in between) for a suitable period of incubation, e.g., 1 minute, 5 minutes, 10 minutes, 15 minutes, 30 minutes, 45 minutes, or 60 minutes, such that the chimeric GH61 polypeptide retains residual activity. However, longer periods of incubation can also be used.

The increased thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof can be determined by differential scanning calorimetry (DSC) using methods standard in the art (see, for example, Sturtevant, 1987, Annual Review of Physical Chemistry 38: 463-488; Example 9 herein). The increased thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof can also be determined using any enzyme assay known in the art for GH61 polypeptides having cellulolytic enhancing activity. See for example, WO 2005/074647, WO 2008/148131 WO 2005/074656, WO 2010/065830, WO 2007/089290, WO 2009/085935, WO 2009/085859, WO 2009/085864, WO 2009/085868, and WO 2008/151043, which are incorporated herein by reference.

One or more (e.g., several) of the parent GH61 polypeptides in which fragments thereof are combined to produce a chimeric GH61 polypeptide may be used to determine the increase in thermostability of the chimeric GH61 polypeptide.

A chimeric GH61 polypeptide with increased thermostability may or may not display increased thermal activity relative to a parent GH61 polypeptide. For example, a chimeric GH61 polypeptide may have increased thermostability relative to a parent GH61 polypeptide thereof, but does not have increased thermal activity.

Isolated: The term “isolated” means a substance in a form or environment that does not occur in nature. Non-limiting examples of isolated substances include (1) any non-naturally occurring substance, (2) any substance including, but not limited to, any enzyme, variant, nucleic acid, protein, peptide or cofactor, that is at least partially removed from one or more or all of the naturally occurring constituents with which it is associated in nature; (3) any substance modified by the hand of man relative to that substance found in nature; or (4) any substance modified by increasing the amount of the substance relative to other components with which it is naturally associated (e.g., multiple copies of a gene encoding the substance; use of a stronger promoter than the promoter naturally associated with the gene encoding the substance). A chimeric GH61 polypeptide of the present invention may be used in industrial applications in the form of a fermentation broth product, that is, the chimeric GH61 polypeptide is a component of a fermentation broth used as a product in industrial applications (e.g., ethanol production). The fermentation broth product will, in addition to the chimeric GH61 polypeptide, comprise additional ingredients used in the fermentation process, such as, for example, cells (including, the host cells containing the gene encoding the chimeric GH61 polypeptide, which are used to produce the polypeptide of interest), cell debris, biomass, fermentation media and/or fermentation products. The fermentation broth may be optionally subjected to one or more purification (including filtration) steps to remove or reduce one more components of a fermentation process. Accordingly, an isolated substance may be present in such a fermentation broth product.

Low stringency conditions: The term “low stringency conditions” means for probes of at least 100 nucleotides in length, prehybridization and hybridization at 42° C. in 5×SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 25% formamide, following standard Southern blotting procedures for 12 to 24 hours. The carrier material is finally washed three times each for 15 minutes using 2×SSC, 0.2% SDS at 50° C.

Mature polypeptide: The term “mature polypeptide” means a polypeptide in its final form following translation and any post-translational modifications, such as N-terminal processing, C-terminal truncation, glycosylation, phosphorylation, etc. It is known in the art that a host cell may produce a mixture of two of more different mature polypeptides (i.e., with a different C-terminal and/or N-terminal amino acid) expressed by the same polynucleotide.

Mature polypeptide coding sequence: The term “mature polypeptide coding sequence” means a polynucleotide that encodes a mature polypeptide having biological activity.

Medium stringency conditions: The term “medium stringency conditions” means for probes of at least 100 nucleotides in length, prehybridization and hybridization at 42° C. in 5×SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 35% formamide, following standard Southern blotting procedures for 12 to 24 hours. The carrier material is finally washed three times each for 15 minutes using 2×SSC, 0.2% SDS at 55° C.

Medium-high stringency conditions: The term “medium-high stringency conditions” means for probes of at least 100 nucleotides in length, prehybridization and hybridization at 42° C. in 5×SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 35% formamide, following standard Southern blotting procedures for 12 to 24 hours. The carrier material is finally washed three times each for 15 minutes using 2×SSC, 0.2% SDS at 60° C.

Nucleic acid construct: The term “nucleic acid construct” means a nucleic acid molecule, either single- or double-stranded, which is isolated from a naturally occurring gene or is modified to contain segments of nucleic acids in a manner that would not otherwise exist in nature or which is synthetic, which comprises one or more control sequences.

Operably linked: The term “operably linked” means a configuration in which a control sequence is placed at an appropriate position relative to the coding sequence of a polynucleotide such that the control sequence directs expression of the coding sequence.

Parent or parent GH61 polypeptide: The term “parent” or “parent GH61 polypeptide” means one of two or more (e.g., several) GH61 polypeptides in which fragments thereof are combined to produce a chimeric GH61 polypeptide of the present invention. The parent may be a naturally occurring (wild-type) polypeptide and/or a variant thereof. The term “parent” or “parent GH61 polypeptide” may also be used in the plural form.

A parent GH61 polypeptide having cellulolytic enhancing activity may be selected from the group consisting of SEQ ID NO: 66, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 72, SEQ ID NO: 74, SEQ ID NO: 76, SEQ ID NO: 78, SEQ ID NO: 80, SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90, SEQ ID NO: 92, SEQ ID NO: 94, SEQ ID NO: 96, SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 110, SEQ ID NO: 112, SEQ ID NO: 114, SEQ ID NO: 116, SEQ ID NO: 118, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 144, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 166, SEQ ID NO: 168, and SEQ ID NO: 170. However, any GH61 polypeptide having cellulolytic enhancing activity may be used in the present invention in accordance with the disclosure herein.

Polypeptide having cellulolytic enhancing activity: The term “polypeptide having cellulolytic enhancing activity” means a GH61 polypeptide that catalyzes the enhancement of the hydrolysis of a cellulosic material by enzyme having cellulolytic activity. For purposes of the present invention, cellulolytic enhancing activity is determined by measuring the increase in reducing sugars or the increase of the total of cellobiose and glucose from the hydrolysis of a cellulosic material by cellulolytic enzyme under the following conditions: 1-50 mg of total protein/g of cellulose in PCS, wherein total protein is comprised of 50-99.5% w/w cellulolytic enzyme protein and 0.5-50% w/w protein of a GH61 polypeptide having cellulolytic enhancing activity for 1-7 days at a suitable temperature, e.g., 50° C., 55° C., or 60° C., and pH, e.g., 5.0 or 5.5, compared to a control hydrolysis with equal total protein loading without cellulolytic enhancing activity (1-50 mg of cellulolytic protein/g of cellulose in PCS). In a preferred aspect, a mixture of CELLUCLAST® 1.5 L (Novozymes A/S, Bagsvrd, Denmark) in the presence of 2-3% of total protein weight Aspergillus oryzae beta-glucosidase (recombinantly produced in Aspergillus oryzae according to WO 02/095014) or 2-3% of total protein weight Aspergillus fumigatus beta-glucosidase (recombinantly produced in Aspergillus oryzae as described in WO 2002/095014) of cellulase protein loading is used as the source of the cellulolytic activity.

The GH61 polypeptides having cellulolytic enhancing activity enhance the hydrolysis of a cellulosic material catalyzed by enzyme having cellulolytic activity by reducing the amount of cellulolytic enzyme required to reach the same degree of hydrolysis preferably at least 1.01-fold, e.g., at least 1.05-fold, at least 1.10-fold, at least 1.25-fold, at least 1.5-fold, at least 2-fold, at least 3-fold, at least 4-fold, at least 5-fold, at least 10-fold, or at least 20-fold.

Pretreated corn stover: The term “PCS” or “Pretreated Corn Stover” means a cellulosic material derived from corn stover by treatment with heat and dilute sulfuric acid, alkaline pretreatment, or neutral pretreatment.

Sequence identity: The relatedness between two amino acid sequences or between two nucleotide sequences is described by the parameter “sequence identity”.

For purposes of the present invention, the sequence identity between two amino acid sequences is determined using the Needleman-Wunsch algorithm (Needleman and Wunsch, 1970, J. Mol. Biol. 48: 443-453) as implemented in the Needle program of the EMBOSS package (EMBOSS: The European Molecular Biology Open Software Suite, Rice et al., 2000, Trends Genet. 16: 276-277), preferably version 3.0.0, 5.0.0, or later. The parameters used are gap open penalty of 10, gap extension penalty of 0.5, and the EBLOSUM62 (EMBOSS version of BLOSUM62) substitution matrix. The output of Needle labeled “longest identity” (obtained using the—nobrief option) is used as the percent identity and is calculated as follows:

(Identical Residues×100)/(Length of Alignment−Total Number of Gaps in Alignment)

For purposes of the present invention, the sequence identity between two deoxyribonucleotide sequences is determined using the Needleman-Wunsch algorithm (Needleman and Wunsch, 1970, supra) as implemented in the Needle program of the EMBOSS package (EMBOSS: The European Molecular Biology Open Software Suite, Rice et al., 2000, supra), preferably version 3.0.0, 5.0.0, or later. The parameters used are gap open penalty of 10, gap extension penalty of 0.5, and the EDNAFULL (EMBOSS version of NCBI NUC4.4) substitution matrix. The output of Needle labeled “longest identity” (obtained using the—nobrief option) is used as the percent identity and is calculated as follows:

(Identical Deoxyribonucleotides×100)/(Length of Alignment−Total Number of Gaps in Alignment)

Subsequence: The term “subsequence” means a polynucleotide having one or more (e.g., several) nucleotides deleted from the 5′- and/or 3′-end of a mature polypeptide coding sequence; wherein the subsequence encodes a fragment having biological activity.

Variant: The term “variant” means a polypeptide having biological activity comprising an alteration, i.e., a substitution, insertion, and/or deletion, at one or more (e.g., several) positions. A substitution means replacement of the amino acid occupying a position with a different amino acid; a deletion means removal of the amino acid occupying a position; and an insertion means adding an amino acid adjacent to and immediately following the amino acid occupying a position.

Very high stringency conditions: The term “very high stringency conditions” means for probes of at least 100 nucleotides in length, prehybridization and hybridization at 42° C. in 5×SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 50% formamide, following standard Southern blotting procedures for 12 to 24 hours. The carrier material is finally washed three times each for 15 minutes using 2×SSC, 0.2% SDS at 70° C.

Very low stringency conditions: The term “very low stringency conditions” means for probes of at least 100 nucleotides in length, prehybridization and hybridization at 42° C. in 5×SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 25% formamide, following standard Southern blotting procedures for 12 to 24 hours. The carrier material is finally washed three times each for 15 minutes using 2×SSC, 0.2% SDS at 45° C.

Xylan-containing material: The term “xylan-containing material” means any material comprising a plant cell wall polysaccharide containing a backbone of beta-(1-4)-linked xylose residues. Xylans of terrestrial plants are heteropolymers possessing a beta-(1-4)-D-xylopyranose backbone, which is branched by short carbohydrate chains. They comprise D-glucuronic acid or its 4-O-methyl ether, L-arabinose, and/or various oligosaccharides, composed of D-xylose, L-arabinose, D- or L-galactose, and D-glucose. Xylan-type polysaccharides can be divided into homoxylans and heteroxylans, which include glucuronoxylans, (arabino)glucuronoxylans, (glucurono)arabinoxylans, arabinoxylans, and complex heteroxylans. See, for example, Ebringerova et al., 2005, Adv. Polym. Sci. 186: 1-67.

In the methods of the present invention, any material containing xylan may be used. In a preferred aspect, the xylan-containing material is lignocellulose.

Xylan degrading activity or xylanolytic activity: The term “xylan degrading activity” or “xylanolytic activity” means a biological activity that hydrolyzes xylan-containing material. The two basic approaches for measuring xylanolytic activity include: (1) measuring the total xylanolytic activity, and (2) measuring the individual xylanolytic activities (e.g., endoxylanases, beta-xylosidases, arabinofuranosidases, alpha-glucuronidases, acetylxylan esterases, feruloyl esterases, and alpha-glucuronyl esterases). Recent progress in assays of xylanolytic enzymes was summarized in several publications including Biely and Puchard, Recent progress in the assays of xylanolytic enzymes, 2006, Journal of the Science of Food and Agriculture 86(11): 1636-1647; Spanikova and Biely, 2006, Glucuronoyl esterase—Novel carbohydrate esterase produced by Schizophyllum commune, FEBS Letters 580(19): 4597-4601; Herrmann, Vrsanska, Jurickova, Hirsch, Biely, and Kubicek, 1997, The beta-D-xylosidase of Trichoderma reesei is a multifunctional beta-D-xylan xylohydrolase, Biochemical Journal 321: 375-381.

Total xylan degrading activity can be measured by determining the reducing sugars formed from various types of xylan, including, for example, oat spelt, beechwood, and larchwood xylans, or by photometric determination of dyed xylan fragments released from various covalently dyed xylans. The most common total xylanolytic activity assay is based on production of reducing sugars from polymeric 4-O-methyl glucuronoxylan as described in Bailey, Biely, Poutanen, 1992, Interlaboratory testing of methods for assay of xylanase activity, Journal of Biotechnology 23(3): 257-270. Xylanase activity can also be determined with 0.2% AZCL-arabinoxylan as substrate in 0.01% TRITON® X-100 (4-(1,1,3,3-tetramethylbutyl)phenyl-polyethylene glycol) and 200 mM sodium phosphate buffer pH 6 at 37° C. One unit of xylanase activity is defined as 1.0 μmole of azurine produced per minute at 37° C., pH 6 from 0.2% AZCL-arabinoxylan as substrate in 200 mM sodium phosphate pH 6 buffer.

For purposes of the present invention, xylan degrading activity is determined by measuring the increase in hydrolysis of birchwood xylan (Sigma Chemical Co., Inc., St. Louis, Mo., USA) by xylan-degrading enzyme(s) under the following typical conditions: 1 ml reactions, 5 mg/ml substrate (total solids), 5 mg of xylanolytic protein/g of substrate, 50 mM sodium acetate pH 5, 50° C., 24 hours, sugar analysis using p-hydroxybenzoic acid hydrazide (PHBAH) assay as described by Lever, 1972, A new reaction for colorimetric determination of carbohydrates, Anal. Biochem 47: 273-279.

Xylanase: The term “xylanase” means a 1,4-beta-D-xylan-xylohydrolase (E.C. 3.2.1.8) that catalyzes the endohydrolysis of 1,4-beta-D-xylosidic linkages in xylans. For purposes of the present invention, xylanase activity is determined with 0.2% AZCL-arabinoxylan as substrate in 0.01% TRITON® X-100 and 200 mM sodium phosphate buffer pH 6 at 37° C. One unit of xylanase activity is defined as 1.0 μmole of azurine produced per minute at 37° C., pH 6 from 0.2% AZCL-arabinoxylan as substrate in 200 mM sodium phosphate pH 6 buffer.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to isolated chimeric GH61 polypeptides having cellulolytic enhancing activity, comprising:

(a) a first GH61 polypeptide fragment at the N-terminal end of the chimeric GH61 polypeptide selected from the group consisting of (i) a polypeptide fragment having at least 60% sequence identity to amino acids 22 to 84 of SEQ ID NO: 78; (ii) a polypeptide fragment encoded by a polynucleotide that hybridizes under at least low stringency conditions with nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polypeptide fragment encoded by a polynucleotide having at least 60% sequence identity to nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof; and (iv) a polypeptide fragment comprising or consisting of amino acids 22 to 84 of SEQ ID NO: 78;

(b) a second GH61 polypeptide fragment at the C-terminal end of the first polypeptide fragment selected from the group consisting of (i) a polypeptide fragment having at least 60% sequence identity to amino acids 85 to 207 of SEQ ID NO: 94; (ii) a polypeptide fragment encoded by a polynucleotide that hybridizes under at least low stringency conditions with nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polypeptide fragment encoded by a polynucleotide having at least 60% sequence identity to nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof; and (iv) a polypeptide fragment comprising or consisting of amino acids 85 to 207 of SEQ ID NO: 94; and

(c) a third GH61 polypeptide fragment at the C-terminal end of the second polypeptide fragment selected from the group consisting of (i) a polypeptide fragment having at least 60% sequence identity to amino acids 208 to 249 of SEQ ID NO: 78; (ii) a polypeptide fragment encoded by a polynucleotide that hybridizes under at least low stringency conditions with nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polypeptide fragment encoded by a polynucleotide having at least 60% sequence identity to nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof; and (iv) a polypeptide fragment comprising or consisting of amino acids 208 to 249 of SEQ ID NO: 78.

In a first aspect, the first GH61 polypeptide fragment at the N-terminal end of the chimeric GH61 polypeptide has a sequence identity to amino acids 22 to 84 of SEQ ID NO: 78 of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%. In one embodiment, the first polypeptide fragment differs by up to 10 amino acids, e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, from amino acids 22 to 84 of SEQ ID NO: 78.

In another embodiment, the first GH61 polypeptide fragment is at least 30 amino acids, e.g., at least 35, at least 40, at least 45, at least 50, at least 55, at least 60, at least 65, at least 70, at least 75, at least 80, at least 85, at least 90, or at least 95 amino acids. In another embodiment, the first GH61 polypeptide fragment is 63 amino acids.

In another embodiment, the first GH61 polypeptide fragment comprises or consists of amino acids 22 to 84 of SEQ ID NO: 78 or an allelic variant thereof; or is a fragment thereof. In another aspect, the first GH61 polypeptide fragment comprises or consists of amino acids 22 to 84 of SEQ ID NO: 78.

In another first aspect, the second GH61 polypeptide fragment at the C-terminal end of the first polypeptide fragment has a sequence identity to amino acids 85 to 207 of SEQ ID NO: 94 of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%. In one embodiment, the second polypeptide fragment differs by up to 10 amino acids, e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, from amino acids 85 to 207 of SEQ ID NO: 94.

In another embodiment, the second GH61 polypeptide fragment is at least 60 amino acids, e.g., at least 65, at least 70, at least 75, at least 85, at least 90, at least 95, at least 100, at least 105, at least 110, at least 115, at least 120, at least 125, at least 130, at least 135, at least 140, at least 145, at least 150, at least 155, at least 160, at least 165, at least 170, at least 175, or at least 180 amino acids. In another embodiment, the second GH61 polypeptide fragment is 123 amino acids.

In another embodiment, the second GH61 polypeptide fragment comprises or consists of amino acids 85 to 207 of SEQ ID NO: 94 or an allelic variant thereof; or is a fragment thereof. In another embodiment, the second GH61 polypeptide fragment comprises or consists of amino acids 85 to 207 of SEQ ID NO: 94.

In another first aspect, the third GH61 polypeptide fragment at the C-terminal end of the second polypeptide fragment has a sequence identity to amino acids 208 to 249 of SEQ ID NO: 78 of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%. In one embodiment, the third polypeptide fragment differs by up to 10 amino acids, e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, from amino acids 208 to 249 of SEQ ID NO: 78.

In another embodiment, the second GH61 polypeptide fragment is at least 20 amino acids, e.g., at least 25, at least 30, at least 35, at least 40, at least 45, at least 50, at least 55 or at least 60 amino acids. In another embodiment, the second GH61 polypeptide fragment is 42 amino acids.

In another embodiment, the third GH61 polypeptide fragment comprises or consists of amino acids 208 to 249 of SEQ ID NO: 78 or an allelic variant thereof; or is a fragment thereof. In another embodiment, the third GH61 polypeptide fragment comprises or consists of amino acids 208 to 249 of SEQ ID NO: 78.

In a second aspect, the first GH61 polypeptide fragment is encoded by a polynucleotide that hybridizes under very low stringency conditions, low stringency conditions, medium stringency conditions, medium-high stringency conditions, high stringency conditions, or very high stringency conditions with (i) nucleotides 64 to 301 of SEQ ID NO: 77, (ii) the cDNA sequence of nucleotides 64 to 301 of SEQ ID NO: 77, or (iii) the full-length complement of (i) or (ii) (J. Sambrook, E. F. Fritsch, and T. Maniatis, 1989, Molecular Cloning, A Laboratory Manual, 2d edition, Cold Spring Harbor, N.Y.).

In another second aspect, the second GH61 polypeptide fragment is encoded by a polynucleotide that hybridizes under very low stringency conditions, low stringency conditions, medium stringency conditions, medium-high stringency conditions, high stringency conditions, or very high stringency conditions with (i) nucleotides 306 to 730 of SEQ ID NO: 93, (ii) the cDNA sequence of nucleotides 306 to 730 of SEQ ID NO: 93, or (iii) the full-length complement of (i) or (ii) (Sambrook et al., 1989, supra).

In another second aspect, the third GH61 polypeptide fragment is encoded by a polynucleotide that hybridizes under very low stringency conditions, low stringency conditions, medium stringency conditions, medium-high stringency conditions, high stringency conditions, or very high stringency conditions with (i) nucleotides 671 to 796 of SEQ ID NO: 77, (ii) the cDNA sequence of nucleotides 671 to 796 of SEQ ID NO: 77, or (iii) the full-length complement of (i) or (ii) (Sambrook et al., 1989, supra).

Nucleotides 64 to 301 of SEQ ID NO: 77, nucleotides 306 to 730 of SEQ ID NO: 93, or nucleotides 671 to 796 of SEQ ID NO: 77, or subsequences thereof, as well as amino acids 22 to 84 of SEQ ID NO: 78, amino acids 85 to 207 of SEQ ID NO: 94, or amino acids 208 to 249 of SEQ ID NO: 78, or fragments thereof, may be used to design nucleic acid probes to identify and clone DNA encoding polypeptides having cellulolytic enhancing activity from strains of different genera or species according to methods well known in the art. In particular, such probes can be used for hybridization with the genomic DNA or cDNA of the genus or species of interest, following standard Southern blotting procedures, in order to identify and isolate the corresponding gene therein. Such probes can be considerably shorter than the entire sequence, but should be at least 15, e.g., at least 25, at least 35, or at least 70 nucleotides in length. Preferably, the nucleic acid probe is at least 100 nucleotides in length, e.g., at least 200 nucleotides, at least 300 nucleotides, at least 400 nucleotides, at least 500 nucleotides, at least 600 nucleotides, at least 700 nucleotides, at least 800 nucleotides, or at least 900 nucleotides in length. Both DNA and RNA probes can be used. The probes are typically labeled for detecting the corresponding gene (for example, with ³²P, ³H, ³⁵S, biotin, or avidin). Such probes are encompassed by the present invention.

A genomic DNA or cDNA library prepared from such other strains may be screened for DNA that hybridizes with the probes described above and encodes a polypeptide having cellulolytic enhancing activity. Genomic or other DNA from such other strains may be separated by agarose or polyacrylamide gel electrophoresis, or other separation techniques. DNA from the libraries or the separated DNA may be transferred to and immobilized on nitrocellulose or other suitable carrier material. In order to identify a clone or DNA, the carrier material is preferably used in a Southern blot.

For purposes of the present invention, hybridization indicates that the polynucleotide hybridizes to a labeled nucleic acid probe corresponding to nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof; nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof; or nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof; or full-length complements thereof; or subsequences thereof; under very low to very high stringency conditions. Molecules to which the nucleic acid probe hybridizes under these conditions can be detected using, for example, X-ray film.

In one embodiment, the nucleic acid probe is nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof. In another embodiment, the nucleic acid probe is nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof. In another embodiment, the nucleic acid probe is nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof. In another embodiment, the nucleic acid probe is a polynucleotide that encodes amino acids 22 to 84 of SEQ ID NO: 78 or a fragment thereof. In another embodiment, the nucleic acid probe is a polynucleotide that encodes amino acids 85 to 207 of SEQ ID NO: 94 or a fragment thereof. In another embodiment, the nucleic acid probe is a polynucleotide that encodes amino acids 208 to 249 of SEQ ID NO: 78 or a fragment thereof.

For short probes of about 15 nucleotides to about 70 nucleotides in length, stringency conditions are defined as prehybridization and hybridization at about 5° C. to about 10° C. below the calculated T_(m) using the calculation according to Bolton and McCarthy (1962, Proc. Natl. Acad. Sci. USA 48:1390) in 0.9 M NaCl, 0.09 M Tris-HCl pH 7.6, 6 mM EDTA, 0.5% NP-40, 1×Denhardt's solution, 1 mM sodium pyrophosphate, 1 mM sodium monobasic phosphate, 0.1 mM ATP, and 0.2 mg of yeast RNA per ml following standard Southern blotting procedures for 12 to 24 hours optimally. The carrier material is finally washed once in 6×SCC plus 0.1% SDS for 15 minutes and twice each for 15 minutes using 6×SSC at 5° C. to 10° C. below the calculated T_(m).

In a third aspect, the first GH61 polypeptide fragment is encoded by a polynucleotide having a sequence identity to nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%.

In another third aspect, the second GH61 polypeptide fragment is encoded by a polynucleotide having a sequence identity to nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%.

In another third aspect, the third GH61 polypeptide fragment is encoded by a polynucleotide having a sequence identity to nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%.

In one embodiment, the chimeric GH61 polypeptide having cellulolytic enhancing activity comprises or consists of SEQ ID NO: 144 or the mature polypeptide thereof. In another embodiment, the chimeric GH61 polypeptide having cellulolytic enhancing activity comprises or consists of amino acids 22 to 249 of SEQ ID NO: 144.

In each of the aspects above, the mature chimeric GH61 polypeptide may further comprise a signal peptide. In one embodiment, the signal peptide is the signal peptide of SEQ ID NO: 78. In another embodiment, the signal peptide is amino acids 1 to 21 of SEQ ID NO: 78.

In another aspect, a chimeric GH61 polypeptide of the present invention has increased thermal activity compared to a parent GH61 polypeptide thereof. In another aspect, a chimeric GH61 polypeptide of the present invention has increased thermostability compared to a parent GH61 polypeptide thereof. In another aspect, a chimeric GH61 polypeptide of the present invention has increased thermal activity and increased thermostability compared to a parent GH61 polypeptide thereof.

In one aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 95° C.

In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 95° C.

In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 95° C.

In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 95° C.

In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 95° C.

In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 95° C.

In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 95° C.

In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 95° C.

In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 95° C.

In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 95° C.

In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 95° C.

In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 95° C.

In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 40° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 45° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 50° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 55° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 60° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 65° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 70° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 75° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 80° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 85° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 90° C. In another aspect, the thermal activity of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 95° C.

In one aspect, the thermal activity of the chimeric GH61 polypeptide is at least 1.01-fold, e.g., at least 1.025-fold, at least 1.05-fold, at least 1.1-fold, at least 1.5-fold, at least 1.8-fold, at least 2-fold, at least 5-fold, at least 10-fold, at least 15-fold, at least 20-fold, at least 25-fold, and at least 50-fold more thermally active than a parent GH61 polypeptide thereof.

In one aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.0 and 95° C.

In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 3.5 and 95° C.

In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.0 and 95° C.

In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 4.5 and 95° C.

In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.0 and 95° C.

In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 5.5 and 95° C.

In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.0 and 95° C.

In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 6.5 and 95° C.

In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.0 and 95° C.

In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 7.5 and 95° C.

In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.0 and 95° C.

In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 8.5 and 95° C.

In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 45° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 50° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 55° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 60° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 65° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 70° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 75° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 80° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 85° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 90° C. In another aspect, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined at pH 9.0 and 95° C.

In each of the aspects above, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined by incubating the chimeric GH61 polypeptide and the parent GH61 polypeptide for 1 minute. In each of the aspects above, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined by incubating the chimeric GH61 polypeptide and the parent GH61 polypeptide for 5 minutes. In each of the aspects above, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined by incubating the chimeric GH61 polypeptide and the parent GH61 polypeptide for 10 minutes. In each of the aspects above, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined by incubating the chimeric GH61 polypeptide and the parent GH61 polypeptide for 15 minutes. In each of the aspects above, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined by incubating the chimeric GH61 polypeptide and the parent GH61 polypeptide for 30 minutes. In each of the aspects above, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined by incubating the chimeric GH61 polypeptide and the parent GH61 polypeptide for 45 minutes. In each of the aspects above, the thermostability of the chimeric GH61 polypeptide relative to a parent GH61 polypeptide thereof is determined by incubating the chimeric GH61 polypeptide and the parent GH61 polypeptide for 60 minutes.

In one aspect, the thermostability of the chimeric GH61 polypeptide having cellulolytic enhancing activity is at least 1.01-fold, e.g., at least 1.025-fold. at least 1.05-fold, at least 1.1-fold, at least 1.5-fold, at least 1.8-fold, at least 2-fold, at least 5-fold, at least 10-fold, at least 15-fold, at least 20-fold, at least 25-fold, and at least 50-fold more thermostable than a parent GH61 polypeptide thereof.

Polynucleotides

The present invention also relates to isolated polynucleotides encoding chimeric GH61 polypeptides having cellulolytic enhancing activity, comprising:

(a) a first polynucleotide encoding a first GH61 polypeptide fragment at the N-terminal end of the chimeric GH61 polypeptide selected from the group consisting of (i) a polynucleotide encoding a polypeptide fragment having at least 60% sequence identity to amino acids 22 to 84 of SEQ ID NO: 78; (ii) a polynucleotide encoding a polypeptide fragment that hybridizes under at least low stringency conditions with nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polynucleotide encoding a polypeptide fragment having at least 60% sequence identity to nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof; and (iv) a polynucleotide encoding a polypeptide fragment comprising or consisting of amino acids 22 to 84 of SEQ ID NO: 78;

(b) a second polynucleotide encoding a second GH61 polypeptide fragment at the C-terminal end of the first polypeptide fragment selected from the group consisting of (i) a polynucleotide encoding a polypeptide fragment having at least 60% sequence identity to amino acids 85 to 207 of SEQ ID NO: 94; (ii) a polynucleotide encoding a polypeptide fragment that hybridizes under at least low stringency conditions with nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polynucleotide encoding a polypeptide fragment having at least 60% sequence identity to nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof; and (iv) a polynucleotide encoding a polypeptide fragment comprising or consisting of amino acids 85 to 207 of SEQ ID NO: 94; and

(c) a third polynucleotide encoding a third GH61 polypeptide fragment at the C-terminal end of the second polypeptide fragment selected from the group consisting of (i) a polynucleotide encoding a polypeptide fragment having at least 60% sequence identity to amino acids 208 to 249 of SEQ ID NO: 78; (ii) a polynucleotide encoding a polypeptide fragment that hybridizes under at least low stringency conditions with nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polynucleotide encoding a polypeptide fragment having at least 60% sequence identity to nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof; and (iv) a polynucleotide encoding a polypeptide fragment comprising or consisting of amino acids 208 to 249 of SEQ ID NO: 78.

In a first aspect, the first polynucleotide encodes the first GH61 polypeptide fragment having a sequence identity to amino acids 22 to 84 of SEQ ID NO: 78 of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%.

In another first aspect, the second polynucleotide encodes the second GH61 polypeptide fragment at the C-terminal end of the first polypeptide fragment having a sequence identity to amino acids 85 to 207 of SEQ ID NO: 94 of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%.

In another first aspect, the third polynucleotide encodes the third GH61 polypeptide fragment having a sequence identity to amino acids 208 to 249 of SEQ ID NO: 78 of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%.

In a second aspect, the first polynucleotide encoding the first GH61 polypeptide fragment hybridizes under very low stringency conditions, low stringency conditions, medium stringency conditions, medium-high stringency conditions, high stringency conditions, or very high stringency conditions with (i) nucleotides 64 to 301 of SEQ ID NO: 77, (ii) the cDNA sequence of nucleotides 64 to 301 of SEQ ID NO: 77, or (iii) the full-length complement of (i) or (ii) (Sambrook et al., 1989, supra).

In another second aspect, the second polynucleotide encoding the second GH61 polypeptide fragment hybridizes under very low stringency conditions, low stringency conditions, medium stringency conditions, medium-high stringency conditions, high stringency conditions, or very high stringency conditions with (i) nucleotides 306 to 730 of SEQ ID NO: 93, (ii) the cDNA sequence of nucleotides 306 to 730 of SEQ ID NO: 93, or (iii) the full-length complement of (i) or (ii) (Sambrook et al., 1989, supra).

In another second aspect, the third polynucleotide encoding the third GH61 polypeptide fragment hybridizes under very low stringency conditions, low stringency conditions, medium stringency conditions, medium-high stringency conditions, high stringency conditions, or very high stringency conditions with (i) nucleotides 671 to 796 of SEQ ID NO: 77, (ii) the cDNA sequence of nucleotides 671 to 796 of SEQ ID NO: 77, or (iii) the full-length complement of (i) or (ii) (Sambrook et al., 1989, supra).

In a third aspect, the first polynucleotide encoding the first GH61 polypeptide fragment has a sequence identity to nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%. In one embodiment, the first polynucleotide comprises or consists of nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof.

In another third aspect, the second polynucleotide encoding the second GH61 polypeptide fragment has a sequence identity to nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%. In one embodiment, the second polynucleotide comprises or consists of nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof.

In another third aspect, the third polynucleotide encoding the third GH61 polypeptide fragment has a sequence identity to nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%. In one embodiment, the third polynucleotide comprises or consists of nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof.

In one embodiment, the chimeric GH61 polypeptide having cellulolytic enhancing activity is encoded by a polynucleotide comprising or consisting of SEQ ID NO: 143 or the mature polypeptide coding sequence thereof; or the cDNA thereof. In another embodiment, the chimeric GH61 polypeptide having cellulolytic enhancing activity is encoded by a polynucleotide comprising or consisting of nucleotides 64 to 852 of SEQ ID NO: 143. In another embodiment, the chimeric GH61 polypeptide having cellulolytic enhancing activity comprises or consists of the mature polypeptide of SEQ ID NO: 144. In another embodiment, the chimeric GH61 polypeptide having cellulolytic enhancing activity comprises or consists of amino acids 22 to 249 of SEQ ID NO: 144.

In each of the embodiment above, the mature chimeric GH61 polypeptide coding sequence may further comprise a signal peptide coding sequence. In one embodiment, the signal peptide is the signal peptide of SEQ ID NO: 78. In another embodiment, the signal peptide is amino acids 1 to 21 of SEQ ID NO: 78. In another embodiment, the signal peptide coding sequence is the signal peptide coding sequence of SEQ ID NO: 77. In another embodiment, the signal peptide coding sequence is nucleotides 1 to 63 of SEQ ID NO: 77.

Nucleic Acid Constructs

The present invention also relates to nucleic acid constructs comprising a polynucleotide encoding a chimeric GH61 polypeptide of the present invention operably linked to one or more control sequences that direct the expression of the coding sequence in a suitable host cell under conditions compatible with the control sequences.

The polynucleotide may be manipulated in a variety of ways to provide for expression of the chimeric GH61 polypeptide. Manipulation of the polynucleotide prior to its insertion into a vector may be desirable or necessary depending on the expression vector. The techniques for modifying polynucleotides utilizing recombinant DNA methods are well known in the art.

The control sequence may be a promoter, a polynucleotide that is recognized by a host cell for expression of a polynucleotide encoding a chimeric GH61 polypeptide of the present invention. The promoter contains transcriptional control sequences that mediate the expression of the polypeptide. The promoter may be any polynucleotide that shows transcriptional activity in the host cell including mutant, truncated, and hybrid promoters, and may be obtained from genes encoding extracellular or intracellular polypeptides either homologous or heterologous to the host cell.

Examples of suitable promoters for directing transcription of the nucleic acid constructs of the present invention in a bacterial host cell are the promoters obtained from the Bacillus amyloliquefaciens alpha-amylase gene (amyQ), Bacillus licheniformis alpha-amylase gene (amyL), Bacillus licheniformis penicillinase gene (penP), Bacillus stearothermophilus maltogenic amylase gene (amyM), Bacillus subtilis levansucrase gene (sacB), Bacillus subtilis xylA and xylB genes, Bacillus thuringiensis ctyIIIA gene (Agaisse and Lereclus, 1994, Molecular Microbiology 13: 97-107), E. coli lac operon, E. coli trc promoter (Egon et al., 1988, Gene 69: 301-315), Streptomyces coelicolor agarase gene (dagA), and prokaryotic beta-lactamase gene (VIIIa-Kamaroff et al., 1978, Proc. Natl. Acad. Sci. USA 75: 3727-3731), as well as the tac promoter (DeBoer et al., 1983, Proc. Natl. Acad. Sci. USA 80: 21-25). Further promoters are described in “Useful proteins from recombinant bacteria” in Gilbert et al., 1980, Scientific American 242: 74-94; and in Sambrook et al., 1989, supra. Examples of tandem promoters are disclosed in WO 99/43835.

Examples of suitable promoters for directing transcription of the nucleic acid constructs of the present invention in a filamentous fungal host cell are promoters obtained from the genes for Aspergillus nidulans acetamidase, Aspergillus niger neutral alpha-amylase, Aspergillus niger acid stable alpha-amylase, Aspergillus niger or Aspergillus awamori glucoamylase (glaA), Aspergillus oryzae TAKA amylase, Aspergillus oryzae alkaline protease, Aspergillus oryzae triose phosphate isomerase, Fusarium oxysporum trypsin-like protease (WO 96/00787), Fusarium venenatum amyloglucosidase (WO 00/56900), Fusarium venenatum Daria (WO 00/56900), Fusarium venenatum Quinn (WO 00/56900), Rhizomucor miehei lipase, Rhizomucor miehei aspartic proteinase, Trichoderma reesei beta-glucosidase, Trichoderma reesei cellobiohydrolase I, Trichoderma reesei cellobiohydrolase II, Trichoderma reesei endoglucanase I, Trichoderma reesei endoglucanase II, Trichoderma reesei endoglucanase III, Trichoderma reesei endoglucanase V, Trichoderma reesei xylanase I, Trichoderma reesei xylanase II, Trichoderma reesei xylanase III, Trichoderma reesei beta-xylosidase, and Trichoderma reesei translation elongation factor, as well as the NA2-tpi promoter (a modified promoter from an Aspergillus neutral alpha-amylase gene in which the untranslated leader has been replaced by an untranslated leader from an Aspergillus triose phosphate isomerase gene; non-limiting examples include modified promoters from an Aspergillus niger neutral alpha-amylase gene in which the untranslated leader has been replaced by an untranslated leader from an Aspergillus nidulans or Aspergillus oryzae triose phosphate isomerase gene); and mutant, truncated, and hybrid promoters thereof. Other promoters are described in U.S. Pat. No. 6,011,147.

In a yeast host, useful promoters are obtained from the genes for Saccharomyces cerevisiae enolase (ENO-1), Saccharomyces cerevisiae galactokinase (GAL1), Saccharomyces cerevisiae alcohol dehydrogenase/glyceraldehyde-3-phosphate dehydrogenase (ADH1, ADH2/GAP), Saccharomyces cerevisiae triose phosphate isomerase (TPI), Saccharomyces cerevisiae metallothionein (CUP1), and Saccharomyces cerevisiae 3-phosphoglycerate kinase. Other useful promoters for yeast host cells are described by Romanos et al., 1992, Yeast 8: 423-488.

The control sequence may also be a transcription terminator, which is recognized by a host cell to terminate transcription. The terminator is operably linked to the 3′-terminus of the polynucleotide encoding the chimeric GH61 polypeptide. Any terminator that is functional in the host cell may be used in the present invention.

Preferred terminators for bacterial host cells are obtained from the genes for Bacillus clausii alkaline protease (aprH), Bacillus licheniformis alpha-amylase (amyL), and Escherichia coli ribosomal RNA (rrnB).

Preferred terminators for filamentous fungal host cells are obtained from the genes for Aspergillus nidulans acetamidase, Aspergillus nidulans anthranilate synthase, Aspergillus niger glucoamylase, Aspergillus niger alpha-glucosidase, Aspergillus oryzae TAKA amylase, Fusarium oxysporum trypsin-like protease, Trichoderma reesei beta-glucosidase, Trichoderma reesei cellobiohydrolase I, Trichoderma reesei cellobiohydrolase II, Trichoderma reesei endoglucanase I, Trichoderma reesei endoglucanase II, Trichoderma reesei endoglucanase III, Trichoderma reesei endoglucanase V, Trichoderma reesei xylanase I, Trichoderma reesei xylanase II, Trichoderma reesei xylanase III, Trichoderma reesei beta-xylosidase, and Trichoderma reesei translation elongation factor.

Preferred terminators for yeast host cells are obtained from the genes for Saccharomyces cerevisiae enolase, Saccharomyces cerevisiae cytochrome C (CYC1), and Saccharomyces cerevisiae glyceraldehyde-3-phosphate dehydrogenase. Other useful terminators for yeast host cells are described by Romanos et al., 1992, supra.

The control sequence may also be an mRNA stabilizer region downstream of a promoter and upstream of the coding sequence of a gene which increases expression of the gene.

Examples of suitable mRNA stabilizer regions are obtained from a Bacillus thuringiensis ctyIIIA gene (WO 94/25612) and a Bacillus subtilis SP82 gene (Hue et al., 1995, Journal of Bacteriology 177: 3465-3471).

The control sequence may also be a leader, a nontranslated region of an mRNA that is important for translation by the host cell. The leader is operably linked to the 5′-terminus of the polynucleotide encoding the chimeric GH61 polypeptide. Any leader that is functional in the host cell may be used.

Preferred leaders for filamentous fungal host cells are obtained from the genes for Aspergillus oryzae TAKA amylase and Aspergillus nidulans triose phosphate isomerase.

Suitable leaders for yeast host cells are obtained from the genes for Saccharomyces cerevisiae enolase (ENO-1), Saccharomyces cerevisiae 3-phosphoglycerate kinase, Saccharomyces cerevisiae alpha-factor, and Saccharomyces cerevisiae alcohol dehydrogenase/glyceraldehyde-3-phosphate dehydrogenase (ADH2/GAP).

The control sequence may also be a polyadenylation sequence, a sequence operably linked to the 3′-terminus of the polynucleotide and, when transcribed, is recognized by the host cell as a signal to add polyadenosine residues to transcribed mRNA. Any polyadenylation sequence that is functional in the host cell may be used.

Preferred polyadenylation sequences for filamentous fungal host cells are obtained from the genes for Aspergillus nidulans anthranilate synthase, Aspergillus niger glucoamylase, Aspergillus niger alpha-glucosidase Aspergillus oryzae TAKA amylase, and Fusarium oxysporum trypsin-like protease.

Useful polyadenylation sequences for yeast host cells are described by Guo and Sherman, 1995, Mol. Cellular Biol. 15: 5983-5990.

The control sequence may also be a signal peptide coding region that encodes a signal peptide linked to the N-terminus of a chimeric GH61 polypeptide of the present invention and directs the polypeptide into the cell's secretory pathway. The 5′-end of the coding sequence of the polynucleotide may inherently contain a signal peptide coding sequence naturally linked in translation reading frame with the segment of the coding sequence that encodes the polypeptide. Alternatively, the 5′-end of the coding sequence may contain a signal peptide coding sequence that is foreign to the coding sequence. A foreign signal peptide coding sequence may be required where the coding sequence does not naturally contain a signal peptide coding sequence. Alternatively, a foreign signal peptide coding sequence may simply replace the natural signal peptide coding sequence in order to enhance secretion of the polypeptide. However, any signal peptide coding sequence that directs the expressed polypeptide into the secretory pathway of a host cell may be used.

Effective signal peptide coding sequences for bacterial host cells are the signal peptide coding sequences obtained from the genes for Bacillus NCIB 11837 maltogenic amylase, Bacillus licheniformis subtilisin, Bacillus licheniformis beta-lactamase, Bacillus stearothermophilus alpha-amylase, Bacillus stearothermophilus neutral proteases (nprT, nprS, nprM), and Bacillus subtilis prsA. Further signal peptides are described by Simonen and Palva, 1993, Microbiological Reviews 57: 109-137.

Effective signal peptide coding sequences for filamentous fungal host cells are the signal peptide coding sequences obtained from the genes for Aspergillus niger neutral amylase, Aspergillus niger glucoamylase, Aspergillus oryzae TAKA amylase, Humicola insolens cellulase, Humicola insolens endoglucanase V, Humicola lanuginosa lipase, and Rhizomucor miehei aspartic proteinase.

Useful signal peptides for yeast host cells are obtained from the genes for Saccharomyces cerevisiae alpha-factor and Saccharomyces cerevisiae invertase. Other useful signal peptide coding sequences are described by Romanos et al., 1992, supra.

The control sequence may also be a propeptide coding sequence that encodes a propeptide positioned at the N-terminus of a chimeric GH61 polypeptide of the present invention. The resultant polypeptide is known as a proenzyme or propolypeptide (or a zymogen in some cases). A propolypeptide is generally inactive and can be converted to an active polypeptide by catalytic or autocatalytic cleavage of the propeptide from the propolypeptide. The propeptide coding sequence may be obtained from the genes for Bacillus subtilis alkaline protease (aprE), Bacillus subtilis neutral protease (nprT), Myceliophthora thermophila laccase (WO 95/33836), Rhizomucor miehei aspartic proteinase, and Saccharomyces cerevisiae alpha-factor.

Where both signal peptide and propeptide sequences are present, the propeptide sequence is positioned next to the N-terminus of a polypeptide and the signal peptide sequence is positioned next to the N-terminus of the propeptide sequence.

It may also be desirable to add regulatory sequences that regulate expression of the chimeric GH61 polypeptide relative to the growth of the host cell. Examples of regulatory sequences are those that cause expression of the gene to be turned on or off in response to a chemical or physical stimulus, including the presence of a regulatory compound. Regulatory sequences in prokaryotic systems include the lac, tac, and trp operator systems. In yeast, the ADH2 system or GAL1 system may be used. In filamentous fungi, the Aspergillus niger glucoamylase promoter, Aspergillus oryzae TAKA alpha-amylase promoter, and Aspergillus oryzae glucoamylase promoter, Trichoderma reesei cellobiohydrolase I promoter, and Trichoderma reesei cellobiohydrolase II promoter may be used. Other examples of regulatory sequences are those that allow for gene amplification. In eukaryotic systems, these regulatory sequences include the dihydrofolate reductase gene that is amplified in the presence of methotrexate, and the metallothionein genes that are amplified with heavy metals. In these cases, the polynucleotide encoding the chimeric GH61 polypeptide would be operably linked to the regulatory sequence.

Expression Vectors

The present invention also relates to recombinant expression vectors comprising a polynucleotide encoding a chimeric GH61 polypeptide of the present invention, a promoter, and transcriptional and translational stop signals. The various nucleotide and control sequences may be joined together to produce a recombinant expression vector that may include one or more convenient restriction sites to allow for insertion or substitution of the polynucleotide encoding the polypeptide at such sites. Alternatively, the polynucleotide may be expressed by inserting the polynucleotide or a nucleic acid construct comprising the polynucleotide into an appropriate vector for expression. In creating the expression vector, the coding sequence is located in the vector so that the coding sequence is operably linked with the appropriate control sequences for expression.

The recombinant expression vector may be any vector (e.g., a plasmid or virus) that can be conveniently subjected to recombinant DNA procedures and can bring about expression of the polynucleotide. The choice of the vector will typically depend on the compatibility of the vector with the host cell into which the vector is to be introduced. The vector may be a linear or closed circular plasmid.

The vector may be an autonomously replicating vector, i.e., a vector that exists as an extrachromosomal entity, the replication of which is independent of chromosomal replication, e.g., a plasmid, an extrachromosomal element, a minichromosome, or an artificial chromosome. The vector may contain any means for assuring self-replication. Alternatively, the vector may be one that, when introduced into the host cell, is integrated into the genome and replicated together with the chromosome(s) into which it has been integrated. Furthermore, a single vector or plasmid or two or more vectors or plasmids that together contain the total DNA to be introduced into the genome of the host cell, or a transposon, may be used.

The vector preferably contains one or more selectable markers that permit easy selection of transformed, transfected, transduced, or the like cells. A selectable marker is a gene the product of which provides for biocide or viral resistance, resistance to heavy metals, prototrophy to auxotrophs, and the like.

Examples of bacterial selectable markers are Bacillus licheniformis or Bacillus subtilis dal genes, or markers that confer antibiotic resistance such as ampicillin, chloramphenicol, kanamycin, neomycin, spectinomycin, or tetracycline resistance. Suitable markers for yeast host cells include, but are not limited to, ADE2, HIS3, LEU2, LYS2, MET3, TRP1, and URA3. Selectable markers for use in a filamentous fungal host cell include, but are not limited to, adeA (phosphoribosylaminoimidazole-succinocarboxamide synthase), adeB (phosphoribosyl-aminoimidazole synthase), amdS (acetamidase), argB (ornithine carbamoyltransferase), bar (phosphinothricin acetyltransferase), hph (hygromycin phosphotransferase), niaD (nitrate reductase), pyrG (orotidine-5′-phosphate decarboxylase), sC (sulfate adenyltransferase), and trpC (anthranilate synthase), as well as equivalents thereof. Preferred for use in an Aspergillus cell are Aspergillus nidulans or Aspergillus oryzae amdS and pyrG genes and a Streptomyces hygroscopicus bar gene. Preferred for use in a Trichoderma cell are adeA, adeB, amdS, hph, and pyrG genes.

The selectable marker may be a dual selectable marker system as described in WO 2010/039889. In one aspect, the dual selectable marker is a hph-tk dual selectable marker system.

The vector preferably contains an element(s) that permits integration of the vector into the host cell's genome or autonomous replication of the vector in the cell independent of the genome.

For integration into the host cell genome, the vector may rely on the polynucleotide's sequence encoding the chimeric GH61 polypeptide or any other element of the vector for integration into the genome by homologous or non-homologous recombination. Alternatively, the vector may contain additional polynucleotides for directing integration by homologous recombination into the genome of the host cell at a precise location(s) in the chromosome(s). To increase the likelihood of integration at a precise location, the integrational elements should contain a sufficient number of nucleic acids, such as 100 to 10,000 base pairs, 400 to 10,000 base pairs, and 800 to 10,000 base pairs, which have a high degree of sequence identity to the corresponding target sequence to enhance the probability of homologous recombination. The integrational elements may be any sequence that is homologous with the target sequence in the genome of the host cell. Furthermore, the integrational elements may be non-encoding or encoding polynucleotides. On the other hand, the vector may be integrated into the genome of the host cell by non-homologous recombination.

For autonomous replication, the vector may further comprise an origin of replication enabling the vector to replicate autonomously in the host cell in question. The origin of replication may be any plasmid replicator mediating autonomous replication that functions in a cell. The term “origin of replication” or “plasmid replicator” means a polynucleotide that enables a plasmid or vector to replicate in vivo.

Examples of bacterial origins of replication are the origins of replication of plasmids pBR322, pUC19, pACYC177, and pACYC184 permitting replication in E. coli, and pUB110, pE194, pTA1060, and pAMβ1 permitting replication in Bacillus.

Examples of origins of replication for use in a yeast host cell are the 2 micron origin of replication, ARS1, ARS4, the combination of ARS1 and CEN3, and the combination of ARS4 and CEN6.

Examples of origins of replication useful in a filamentous fungal cell are AMA1 and ANSI (Gems et al., 1991, Gene 98: 61-67; Cullen et al., 1987, Nucleic Acids Res. 15: 9163-9175; WO 00/24883). Isolation of the AMA1 gene and construction of plasmids or vectors comprising the gene can be accomplished according to the methods disclosed in WO 00/24883.

More than one copy of a polynucleotide of the present invention may be inserted into a host cell to increase production of a chimeric GH61 polypeptide of the present invention. An increase in the copy number of the polynucleotide can be obtained by integrating at least one additional copy of the sequence into the host cell genome or by including an amplifiable selectable marker gene with the polynucleotide where cells containing amplified copies of the selectable marker gene, and thereby additional copies of the polynucleotide, can be selected for by cultivating the cells in the presence of the appropriate selectable agent.

The procedures used to ligate the elements described above to construct the recombinant expression vectors of the present invention are well known to one skilled in the art (see, e.g., Sambrook et al., 1989, supra).

Host Cells

The present invention also relates to recombinant host cells, comprising a polynucleotide encoding a chimeric GH61 polypeptide of the present invention operably linked to one or more control sequences that direct the production of the polypeptide. A construct or vector comprising a polynucleotide is introduced into a host cell so that the construct or vector is maintained as a chromosomal integrant or as a self-replicating extra-chromosomal vector as described earlier. The term “host cell” encompasses any progeny of a parent cell that is not identical to the parent cell due to mutations that occur during replication.

The host cell may be any cell useful in the recombinant production of a chimeric GH61 polypeptide of the present invention, e.g., a prokaryote or a eukaryote.

The prokaryotic host cell may be any Gram-positive or Gram-negative bacterium. Gram-positive bacteria include, but are not limited to, Bacillus, Clostridium, Enterococcus, Geobacillus, Lactobacillus, Lactococcus, Oceanobacillus, Staphylococcus, Streptococcus, and Streptomyces. Gram-negative bacteria include, but are not limited to, Campylobacter, E. coli, Flavobacterium, Fusobacterium, Helicobacter, Ilyobacter, Neisseria, Pseudomonas, Salmonella, and Ureaplasma.

The bacterial host cell may be any Bacillus cell including, but not limited to, Bacillus alkalophilus, Bacillus amyloliquefaciens, Bacillus brevis, Bacillus circulans, Bacillus clausii, Bacillus coagulans, Bacillus firmus, Bacillus lautus, Bacillus lentus, Bacillus licheniformis, Bacillus megaterium, Bacillus pumilus, Bacillus stearothermophilus, Bacillus subtilis, and Bacillus thuringiensis cells.

The bacterial host cell may also be any Streptococcus cell including, but not limited to, Streptococcus equisimilis, Streptococcus pyogenes, Streptococcus uberis, and Streptococcus equi subsp. Zooepidemicus cells.

The bacterial host cell may also be any Streptomyces cell including, but not limited to, Streptomyces achromogenes, Streptomyces avermitilis, Streptomyces coelicolor, Streptomyces griseus, and Streptomyces lividans cells.

The introduction of DNA into a Bacillus cell may be effected by protoplast transformation (see, e.g., Chang and Cohen, 1979, Mol. Gen. Genet. 168: 111-115), competent cell transformation (see, e.g., Young and Spizizen, 1961, J. Bacteriol. 81: 823-829, or Dubnau and Davidoff-Abelson, 1971, J. Mol. Biol. 56: 209-221), electroporation (see, e.g., Shigekawa and Dower, 1988, Biotechniques 6: 742-751), or conjugation (see, e.g., Koehler and Thorne, 1987, J. Bacteriol. 169: 5271-5278). The introduction of DNA into an E. coli cell may be effected by protoplast transformation (see, e.g., Hanahan, 1983, J. Mol. Biol. 166: 557-580) or electroporation (see, e.g., Dower et al., 1988, Nucleic Acids Res. 16: 6127-6145). The introduction of DNA into a Streptomyces cell may be effected by protoplast transformation, electroporation (see, e.g., Gong et al., 2004, Folia Microbiol. (Praha) 49: 399-405), conjugation (see, e.g., Mazodier et al., 1989, J. Bacteriol. 171: 3583-3585), or transduction (see, e.g., Burke et al., 2001, Proc. Natl. Acad. Sci. USA 98: 6289-6294). The introduction of DNA into a Pseudomonas cell may be effected by electroporation (see, e.g., Choi et al., 2006, J. Microbiol. Methods 64: 391-397) or conjugation (see, e.g., Pinedo and Smets, 2005, Appl. Environ. Microbiol. 71: 51-57). The introduction of DNA into a Streptococcus cell may be effected by natural competence (see, e.g., Perry and Kuramitsu, 1981, Infect. Immun. 32: 1295-1297), protoplast transformation (see, e.g., Catt and Jollick, 1991, Microbios 68: 189-207), electroporation (see, e.g., Buckley et al., 1999, Appl. Environ. Microbiol. 65: 3800-3804), or conjugation (see, e.g., Clewell, 1981, Microbiol. Rev. 45: 409-436). However, any method known in the art for introducing DNA into a host cell can be used.

The host cell may also be a eukaryote, such as a mammalian, insect, plant, or fungal cell.

The host cell may be a fungal cell. “Fungi” as used herein includes the phyla Ascomycota, Basidiomycota, Chytridiomycota, and Zygomycota as well as the Oomycota and all mitosporic fungi (as defined by Hawksworth et al., In, Ainsworth and Bisby's Dictionary of The Fungi, 8th edition, 1995, CAB International, University Press, Cambridge, UK).

The fungal host cell may be a yeast cell. “Yeast” as used herein includes ascosporogenous yeast (Endomycetales), basidiosporogenous yeast, and yeast belonging to the Fungi Imperfecti (Blastomycetes). Since the classification of yeast may change in the future, for the purposes of this invention, yeast shall be defined as described in Biology and Activities of Yeast (Skinner, Passmore, and Davenport, editors, Soc. App. Bacteriol. Symposium Series No. 9, 1980).

The yeast host cell may be a Candida, Hansenula, Kluyveromyces, Pichia, Saccharomyces, Schizosaccharomyces, or Yarrowia cell, such as a Kluyveromyces lactis, Saccharomyces carlsbergensis, Saccharomyces cerevisiae, Saccharomyces diastaticus, Saccharomyces douglasii, Saccharomyces kluyveri, Saccharomyces norbensis, Saccharomyces oviformis, or Yarrowia lipolytica cell.

The fungal host cell may be a filamentous fungal cell. “Filamentous fungi” include all filamentous forms of the subdivision Eumycota and Oomycota (as defined by Hawksworth et al., 1995, supra). The filamentous fungi are generally characterized by a mycelial wall composed of chitin, cellulose, glucan, chitosan, mannan, and other complex polysaccharides. Vegetative growth is by hyphal elongation and carbon catabolism is obligately aerobic. In contrast, vegetative growth by yeasts such as Saccharomyces cerevisiae is by budding of a unicellular thallus and carbon catabolism may be fermentative.

The filamentous fungal host cell may be an Acremonium, Aspergillus, Aureobasidium, Bjerkandera, Ceriporiopsis, Chrysosporium, Coprinus, Coriolus, Cryptococcus, Filibasidium, Fusarium, Humicola, Magnaporthe, Mucor, Myceliophthora, Neocallimastix, Neurospora, Paecilomyces, Penicillium, Phanerochaete, Phlebia, Piromyces, Pleurotus, Schizophyllum, Talaromyces, Thermoascus, Thielavia, Tolypocladium, Trametes, or Trichoderma cell.

For example, the filamentous fungal host cell may be an Aspergillus awamori, Aspergillus foetidus, Aspergillus fumigatus, Aspergillus japonicus, Aspergillus nidulans, Aspergillus niger, Aspergillus oryzae, Bjerkandera adusta, Ceriporiopsis aneirina, Ceriporiopsis caregiea, Ceriporiopsis gilvescens, Ceriporiopsis pannocinta, Ceriporiopsis rivulosa, Ceriporiopsis subrufa, Ceriporiopsis subvermispora, Chrysosporium inops, Chrysosporium keratinophilum, Chrysosporium lucknowense, Chrysosporium merdarium, Chrysosporium pannicola, Chrysosporium queenslandicum, Chrysosporium tropicum, Chrysosporium zonatum, Coprinus cinereus, Coriolus hirsutus, Fusarium bactridioides, Fusarium cerealis, Fusarium crookwellense, Fusarium culmorum, Fusarium graminearum, Fusarium graminum, Fusarium heterosporum, Fusarium negundi, Fusarium oxysporum, Fusarium reticulatum, Fusarium roseum, Fusarium sambucinum, Fusarium sarcochroum, Fusarium sporotrichioides, Fusarium sulphureum, Fusarium torulosum, Fusarium trichothecioides, Fusarium venenatum, Humicola insolens, Humicola lanuginosa, Mucor miehei, Myceliophthora thermophila, Neurospora crassa, Penicillium purpurogenum, Phanerochaete chrysosporium, Phlebia radiata, Pleurotus eryngii, Thielavia terrestris, Trametes villosa, Trametes versicolor, Trichoderma harzianum, Trichoderma koningii, Trichoderma longibrachiatum, Trichoderma reesei, or Trichoderma viride cell.

Fungal cells may be transformed by a process involving protoplast formation, transformation of the protoplasts, and regeneration of the cell wall in a manner known per se. Suitable procedures for transformation of Aspergillus and Trichoderma host cells are described in EP 238023, Yelton et al., 1984, Proc. Natl. Acad. Sci. USA 81: 1470-1474, and Christensen et al., 1988, Bio/Technology 6: 1419-1422. Suitable methods for transforming Fusarium species are described by Malardier et al., 1989, Gene 78: 147-156, and WO 96/00787. Yeast may be transformed using the procedures described by Becker and Guarente, In Abelson, J. N. and Simon, M. I., editors, Guide to Yeast Genetics and Molecular Biology, Methods in Enzymology, Volume 194, pp 182-187, Academic Press, Inc., New York; Ito et al., 1983, J. Bacteriol. 153: 163; and Hinnen et al., 1978, Proc. Natl. Acad. Sci. USA 75: 1920.

Methods of Production

The present invention also relates to methods of producing a chimeric GH61 polypeptide, comprising: (a) cultivating a host cell of the present invention under conditions suitable for the expression of the chimeric GH61 polypeptide; and (b) recovering the chimeric GH61 polypeptide.

The cells are cultivated in a nutrient medium suitable for production of the chimeric GH61 polypeptide using methods known in the art. For example, the cells may be cultivated by shake flask cultivation, or small-scale or large-scale fermentation (including continuous, batch, fed-batch, or solid state fermentations) in laboratory or industrial fermentors in a suitable medium and under conditions allowing the polypeptide to be expressed and/or isolated. The cultivation takes place in a suitable nutrient medium comprising carbon and nitrogen sources and inorganic salts, using procedures known in the art. Suitable media are available from commercial suppliers or may be prepared according to published compositions (e.g., in catalogues of the American Type Culture Collection). If the polypeptide is secreted into the nutrient medium, the polypeptide can be recovered directly from the medium. If the polypeptide is not secreted, it can be recovered from cell lysates.

The chimeric GH61 polypeptide may be detected using methods known in the art that are specific for the chimeric GH61 polypeptides. These detection methods may include use of specific antibodies, formation of an enzyme product, or disappearance of an enzyme substrate. For example, an enzyme assay may be used to determine the activity of the chimeric GH61 polypeptide.

The chimeric GH61 polypeptide may be recovered by methods known in the art. For example, the polypeptide may be recovered from the nutrient medium by conventional procedures including, but not limited to, collection, centrifugation, filtration, extraction, spray-drying, evaporation, or precipitation. In one aspect, the whole fermentation broth is recovered.

The chimeric GH61 polypeptide may be purified by a variety of procedures known in the art including, but not limited to, chromatography (e.g., ion exchange, affinity, hydrophobic, chromatofocusing, and size exclusion), electrophoretic procedures (e.g., preparative isoelectric focusing), differential solubility (e.g., ammonium sulfate precipitation), SDS-PAGE, or extraction (see, e.g., Protein Purification, J.-C. Janson and Lars Ryden, editors, VCH Publishers, New York, 1989) to obtain substantially pure chimeric GH61 polypeptides.

In an alternative aspect, the chimeric GH61 polypeptide is not recovered, but rather a host cell of the present invention expressing the polypeptide is used as a source of the polypeptide.

Compositions

The present invention also relates to compositions comprising a chimeric GH61 polypeptide of the present invention. Preferably, the compositions are enriched in such a polypeptide. The term “enriched” indicates that the cellulolytic enhancing activity of the composition has been increased, e.g., with an enrichment factor of at least 1.1.

The compositions may comprise a chimeric GH61 polypeptide of the present invention as the major enzymatic component, e.g., a mono-component composition. Alternatively, the compositions may comprise multiple enzymatic activities, such as one or more (e.g., several) additional enzymes selected from the group consisting of a cellulase, a polypeptide having cellulolytic enhancing activity, a hemicellulase, an esterase, an expansin, a laccase, a ligninolytic enzyme, a pectinase, a peroxidase, a protease, and a swollenin.

The compositions may be prepared in accordance with methods known in the art and may be in the form of a liquid or a dry composition. The compositions may be stabilized in accordance with methods known in the art.

The compositions may be a fermentation broth formulation or a cell composition, as described herein. Consequently, the present invention also relates to fermentation broth formulations and cell compositions comprising a chimeric GH61 polypeptide of the present invention. In some embodiments, the composition is a cell-killed whole broth containing organic acid(s), killed cells and/or cell debris, and culture medium.

The term “fermentation broth” as used herein refers to a preparation produced by cellular fermentation that undergoes no or minimal recovery and/or purification. For example, fermentation broths are produced when microbial cultures are grown to saturation, incubated under carbon-limiting conditions to allow protein synthesis (e.g., expression of enzymes by host cells) and secretion into cell culture medium. The fermentation broth can contain unfractionated or fractionated contents of the fermentation materials derived at the end of the fermentation. Typically, the fermentation broth is unfractionated and comprises the spent culture medium and cell debris present after the microbial cells (e.g., filamentous fungal cells) are removed, e.g., by centrifugation. In some embodiments, the fermentation broth contains spent cell culture medium, extracellular enzymes, and viable and/or nonviable microbial cells.

In an embodiment, the fermentation broth formulation and cell compositions comprise a first organic acid component comprising at least one 1-5 carbon organic acid and/or a salt thereof and a second organic acid component comprising at least one 6 or more carbon organic acid and/or a salt thereof. In a specific embodiment, the first organic acid component is acetic acid, formic acid, propionic acid, a salt thereof, or a mixture of two or more of the foregoing and the second organic acid component is benzoic acid, cyclohexanecarboxylic acid, 4-methylvaleric acid, phenylacetic acid, a salt thereof, or a mixture of two or more of the foregoing.

In one aspect, the composition contains an organic acid(s), and optionally further contains killed cells and/or cell debris. In one embodiment, the killed cells and/or cell debris are removed from a cell-killed whole broth to provide a composition that is free of these components.

The fermentation broth formulations or cell compostions may further comprise a preservative and/or anti-microbial (e.g., bacteriostatic) agent, including, but not limited to, sorbitol, sodium chloride, potassium sorbate, and others known in the art.

The cell-killed whole broth or composition may further comprise one or more (e.g., several) enzymes such as acetyl xylan esterase, alpha-arabinofuranosidase, alpha-galactosidase, alpha-glucuronidase, amylase, arabinanase, arabinofuranosidase, beta-galactosidase, beta-glucosidase, cellobiohydrolase, endoglucanase, endo-beta-1,3(4)-glucanase, ferrulic acid esterase, galactanase, glucoamylase, glucohydrolase, hybrid peroxidases, with combined properties of lignin peroxidases and manganese-dependent peroxidases, laccase, lignin peroxidase, manganese-dependent peroxidases, mannanase, mannan acetyl esterase, mannosidase, pectate lyase, pectin acetyl esterase, pectinase lyase, pectin methyl esterase, polygalacturonase, protease, rhamnogalacturonan lyase, rhamnogalacturonan acetyl esterase, rhamnogalacturonase, xylanase, xylogalacturonosidase, xylogalacturonase, xyloglucanase, and xylosidase.

In some embodiments, the cell-killed whole broth or composition includes cellulolytic enzymes including, but not limited to, (i) endoglucanases (EG) or 1,4-D-glucan-4-glucanohydrolases (EC 3.2.1.4), (ii) exoglucanases, including 1,4-D-glucan glucanohydrolases (also known as cellodextnnases) (EC 3.2.1.74) and 1,4-D-glucan cellobiohydrolases (exo-cellobiohydrolases, CBH) (EC 3.2.1.91), and (iii) beta-glucosidase (BG) or beta-glucoside glucohydrolases (EC 3.2.1.21).

The cell-killed whole broth or composition may contain the unfractionated contents of the fermentation materials derived at the end of the fermentation. Typically, the cell-killed whole broth or composition contains the spent culture medium and cell debris present after the microbial cells (e.g., filamentous fungal cells) are grown to saturation, incubated under carbon-limiting conditions to allow protein synthesis (e.g., expression of cellulase and/or glucosidase enzyme(s)). In some embodiments, the cell-killed whole broth or composition contains the spent cell culture medium, extracellular enzymes, and killed filamentous fungal cells. In some embodiments, the microbial cells present in the cell-killed whole broth or composition can be permeabilized and/or lysed using methods known in the art.

A whole broth or cell composition as described herein is typically a liquid, but may contain insoluble components, such as killed cells, cell debris, culture media components, and/or insoluble enzyme(s). In some embodiments, insoluble components may be removed to provide a clarified liquid composition.

The whole broth formulations and cell compositions of the present invention may be produced by a method described in WO 90/15861 or WO 2010/096673.

Examples are given below of preferred uses of the compositions of the present invention. The dosage of the composition and other conditions under which the composition is used may be determined on the basis of methods known in the art.

Uses

The present invention is also directed to the following methods for using the chimeric GH61 polypeptides, or compositions thereof.

The present invention also relates to methods for degrading a cellulosic material, comprising: treating the cellulosic material with an enzyme composition in the presence of a chimeric GH61 polypeptide having cellulolytic enhancing activity of the present invention. In one aspect, the methods further comprise recovering the degraded or converted cellulosic material. Soluble products of degradation or conversion of the cellulosic material can be separated from insoluble cellulosic material using a method known in the art such as, for example, centrifugation, filtration, or gravity settling.

The present invention also relates to methods of producing a fermentation product, comprising: (a) saccharifying a cellulosic material with an enzyme composition in the presence of a chimeric GH61 polypeptide having cellulolytic enhancing activity of the present invention; (b) fermenting the saccharified cellulosic material with one or more (e.g., several) fermenting microorganisms to produce the fermentation product; and (c) recovering the fermentation product from the fermentation.

The present invention also relates to methods of fermenting a cellulosic material, comprising: fermenting the cellulosic material with one or more (e.g., several) fermenting microorganisms, wherein the cellulosic material is saccharified with an enzyme composition in the presence of a chimeric GH61 polypeptide having cellulolytic enhancing activity of the present invention. In one aspect, the fermenting of the cellulosic material produces a fermentation product. In another aspect, the methods further comprise recovering the fermentation product from the fermentation.

The methods of the present invention can be used to saccharify the cellulosic material to fermentable sugars and to convert the fermentable sugars to many useful fermentation products, e.g., fuel, potable ethanol, and/or platform chemicals (e.g., acids, alcohols, ketones, gases, and the like). The production of a desired fermentation product from the cellulosic material typically involves pretreatment, enzymatic hydrolysis (saccharification), and fermentation.

The processing of the cellulosic material according to the present invention can be accomplished using methods conventional in the art. Moreover, the methods of the present invention can be implemented using any conventional biomass processing apparatus configured to operate in accordance with the invention.

Hydrolysis (saccharification) and fermentation, separate or simultaneous, include, but are not limited to, separate hydrolysis and fermentation (SHF); simultaneous saccharification and fermentation (SSF); simultaneous saccharification and co-fermentation (SSCF); hybrid hydrolysis and fermentation (HHF); separate hydrolysis and co-fermentation (SHCF); hybrid hydrolysis and co-fermentation (HHCF); and direct microbial conversion (DMC), also sometimes called consolidated bioprocessing (CBP). SHF uses separate process steps to first enzymatically hydrolyze the cellulosic material to fermentable sugars, e.g., glucose, cellobiose, and pentose monomers, and then ferment the fermentable sugars to ethanol. In SSF, the enzymatic hydrolysis of the cellulosic material and the fermentation of sugars to ethanol are combined in one step (Philippidis, G. P., 1996, Cellulose bioconversion technology, in Handbook on Bioethanol: Production and Utilization, Wyman, C. E., ed., Taylor & Francis, Washington, D.C., 179-212). SSCF involves the co-fermentation of multiple sugars (Sheehan, J., and Himmel, M., 1999, Enzymes, energy and the environment: A strategic perspective on the U.S. Department of Energy's research and development activities for bioethanol, Biotechnol. Prog. 15: 817-827). HHF involves a separate hydrolysis step, and in addition a simultaneous saccharification and hydrolysis step, which can be carried out in the same reactor. The steps in an HHF process can be carried out at different temperatures, i.e., high temperature enzymatic saccharification followed by SSF at a lower temperature that the fermentation strain can tolerate. DMC combines all three processes (enzyme production, hydrolysis, and fermentation) in one or more (e.g., several) steps where the same organism is used to produce the enzymes for conversion of the cellulosic material to fermentable sugars and to convert the fermentable sugars into a final product (Lynd, L. R., Weimer, P. J., van Zyl, W. H., and Pretorius, I. S., 2002, Microbial cellulose utilization: Fundamentals and biotechnology, Microbiol. Mol. Biol. Reviews 66: 506-577). It is understood herein that any method known in the art comprising pretreatment, enzymatic hydrolysis (saccharification), fermentation, or a combination thereof, can be used in the practicing the methods of the present invention.

A conventional apparatus can include a fed-batch stirred reactor, a batch stirred reactor, a continuous flow stirred reactor with ultrafiltration, and/or a continuous plug-flow column reactor (Fernanda de Castilhos Corazza, Flávio Faria de Moraes, Gisella Maria Zanin and Ivo Neitzel, 2003, Optimal control in fed-batch reactor for the cellobiose hydrolysis, Acta Scientiarum. Technology 25: 33-38; Gusakov, A. V., and Sinitsyn, A. P., 1985, Kinetics of the enzymatic hydrolysis of cellulose: 1. A mathematical model for a batch reactor process, Enz. Microb. Technol. 7: 346-352), an attrition reactor (Ryu, S. K., and Lee, J. M., 1983, Bioconversion of waste cellulose by using an attrition bioreactor, Biotechnol. Bioeng. 25: 53-65), or a reactor with intensive stirring induced by an electromagnetic field (Gusakov, A. V., Sinitsyn, A. P., Davydkin, I. Y., Davydkin, V. Y., Protas, O. V., 1996, Enhancement of enzymatic cellulose hydrolysis using a novel type of bioreactor with intensive stirring induced by electromagnetic field, Appl. Biochem. Biotechnol. 56: 141-153). Additional reactor types include fluidized bed, upflow blanket, immobilized, and extruder type reactors for hydrolysis and/or fermentation.

Pretreatment.

In practicing the methods of the present invention, any pretreatment process known in the art can be used to disrupt plant cell wall components of the cellulosic material (Chandra et al., 2007, Substrate pretreatment: The key to effective enzymatic hydrolysis of lignocellulosics?, Adv. Biochem. Engin./Biotechnol. 108: 67-93; Galbe and Zacchi, 2007, Pretreatment of lignocellulosic materials for efficient bioethanol production, Adv. Biochem. Engin./Biotechnol. 108: 41-65; Hendriks and Zeeman, 2009, Pretreatments to enhance the digestibility of lignocellulosic biomass, Bioresource Technol. 100: 10-18; Mosier et al., 2005, Features of promising technologies for pretreatment of lignocellulosic biomass, Bioresource Technol. 96: 673-686; Taherzadeh and Karimi, 2008, Pretreatment of lignocellulosic wastes to improve ethanol and biogas production: A review, Int. J. of Mol. Sci. 9: 1621-1651; Yang and Wyman, 2008, Pretreatment: the key to unlocking low-cost cellulosic ethanol, Biofuels Bioproducts and Biorefining-Biofpr. 2: 26-40).

The cellulosic material can also be subjected to particle size reduction, sieving, pre-soaking, wetting, washing, and/or conditioning prior to pretreatment using methods known in the art.

Conventional pretreatments include, but are not limited to, steam pretreatment (with or without explosion), dilute acid pretreatment, hot water pretreatment, alkaline pretreatment, lime pretreatment, wet oxidation, wet explosion, ammonia fiber explosion, organosolv pretreatment, and biological pretreatment. Additional pretreatments include ammonia percolation, ultrasound, electroporation, microwave, supercritical CO₂, supercritical H₂O, ozone, ionic liquid, and gamma irradiation pretreatments.

The cellulosic material can be pretreated before hydrolysis and/or fermentation. Pretreatment is preferably performed prior to the hydrolysis. Alternatively, the pretreatment can be carried out simultaneously with enzyme hydrolysis to release fermentable sugars, such as glucose, xylose, and/or cellobiose. In most cases the pretreatment step itself results in some conversion of biomass to fermentable sugars (even in absence of enzymes).

Steam Pretreatment. In steam pretreatment, the cellulosic material is heated to disrupt the plant cell wall components, including lignin, hemicellulose, and cellulose to make the cellulose and other fractions, e.g., hemicellulose, accessible to enzymes. The cellulosic material is passed to or through a reaction vessel where steam is injected to increase the temperature to the required temperature and pressure and is retained therein for the desired reaction time. Steam pretreatment is preferably performed at 140-250° C., e.g., 160-200° C. or 170-190° C., where the optimal temperature range depends on addition of a chemical catalyst. Residence time for the steam pretreatment is preferably 1-60 minutes, e.g., 1-30 minutes, 1-20 minutes, 3-12 minutes, or 4-10 minutes, where the optimal residence time depends on temperature range and addition of a chemical catalyst. Steam pretreatment allows for relatively high solids loadings, so that the cellulosic material is generally only moist during the pretreatment. The steam pretreatment is often combined with an explosive discharge of the material after the pretreatment, which is known as steam explosion, that is, rapid flashing to atmospheric pressure and turbulent flow of the material to increase the accessible surface area by fragmentation (Duff and Murray, 1996, Bioresource Technology 855: 1-33; Galbe and Zacchi, 2002, Appl. Microbiol. Biotechnol. 59: 618-628; U.S. Patent Application No. 20020164730). During steam pretreatment, hemicellulose acetyl groups are cleaved and the resulting acid autocatalyzes partial hydrolysis of the hemicellulose to monosaccharides and oligosaccharides. Lignin is removed to only a limited extent.

Chemical Pretreatment: The term “chemical treatment” refers to any chemical pretreatment that promotes the separation and/or release of cellulose, hemicellulose, and/or lignin. Such a pretreatment can convert crystalline cellulose to amorphous cellulose. Examples of suitable chemical pretreatment processes include, for example, dilute acid pretreatment, lime pretreatment, wet oxidation, ammonia fiber/freeze explosion (AFEX), ammonia percolation (APR), ionic liquid, and organosolv pretreatments.

A catalyst such as H₂SO₄ or SO₂ (typically 0.3 to 5% w/w) is often added prior to steam pretreatment, which decreases the time and temperature, increases the recovery, and improves enzymatic hydrolysis (Ballesteros et al., 2006, Appl. Biochem. Biotechnol. 129-132: 496-508; Varga et al., 2004, Appl. Biochem. Biotechnol. 113-116: 509-523; Sassner et al., 2006, Enzyme Microb. Technol. 39: 756-762). In dilute acid pretreatment, the cellulosic material is mixed with dilute acid, typically H₂SO₄, and water to form a slurry, heated by steam to the desired temperature, and after a residence time flashed to atmospheric pressure. The dilute acid pretreatment can be performed with a number of reactor designs, e.g., plug-flow reactors, counter-current reactors, or continuous counter-current shrinking bed reactors (Duff and Murray, 1996, supra; Schell et al., 2004, Bioresource Technol. 91: 179-188; Lee et al., 1999, Adv. Biochem. Eng. Biotechnol. 65: 93-115).

Several methods of pretreatment under alkaline conditions can also be used. These alkaline pretreatments include, but are not limited to, sodium hydroxide, lime, wet oxidation, ammonia percolation (APR), and ammonia fiber/freeze explosion (AFEX).

Lime pretreatment is performed with calcium oxide or calcium hydroxide at temperatures of 85-150° C. and residence times from 1 hour to several days (Wyman et al., 2005, Bioresource Technol. 96: 1959-1966; Mosier et al., 2005, Bioresource Technol. 96: 673-686). WO 2006/110891, WO 2006/110899, WO 2006/110900, and WO 2006/110901 disclose pretreatment methods using ammonia.

Wet oxidation is a thermal pretreatment performed typically at 180-200° C. for 5-15 minutes with addition of an oxidative agent such as hydrogen peroxide or over-pressure of oxygen (Schmidt and Thomsen, 1998, Bioresource Technol. 64: 139-151; Palonen et al., 2004, Appl. Biochem. Biotechnol. 117: 1-17; Varga et al., 2004, Biotechnol. Bioeng. 88: 567-574; Martin et al., 2006, J. Chem. Technol. Biotechnol. 81: 1669-1677). The pretreatment is performed preferably at 1-40% dry matter, e.g., 2-30% dry matter or 5-20% dry matter, and often the initial pH is increased by the addition of alkali such as sodium carbonate.

A modification of the wet oxidation pretreatment method, known as wet explosion (combination of wet oxidation and steam explosion) can handle dry matter up to 30%. In wet explosion, the oxidizing agent is introduced during pretreatment after a certain residence time. The pretreatment is then ended by flashing to atmospheric pressure (WO 2006/032282).

Ammonia fiber explosion (AFEX) involves treating the cellulosic material with liquid or gaseous ammonia at moderate temperatures such as 90-150° C. and high pressure such as 17-20 bar for 5-10 minutes, where the dry matter content can be as high as 60% (Gollapalli et al., 2002, Appl. Biochem. Biotechnol. 98: 23-35; Chundawat et al., 2007, Biotechnol. Bioeng. 96: 219-231; Alizadeh et al., 2005, Appl. Biochem. Biotechnol. 121: 1133-1141; Teymouri et al., 2005, Bioresource Technol. 96: 2014-2018). During AFEX pretreatment cellulose and hemicelluloses remain relatively intact. Lignin-carbohydrate complexes are cleaved.

Organosolv pretreatment delignifies the cellulosic material by extraction using aqueous ethanol (40-60% ethanol) at 160-200° C. for 30-60 minutes (Pan et al., 2005, Biotechnol. Bioeng. 90: 473-481; Pan et al., 2006, Biotechnol. Bioeng. 94: 851-861; Kurabi et al., 2005, Appl. Biochem. Biotechnol. 121: 219-230). Sulphuric acid is usually added as a catalyst. In organosolv pretreatment, the majority of hemicellulose and lignin is removed.

Other examples of suitable pretreatment methods are described by Schell et al., 2003, Appl. Biochem. and Biotechnol. Vol. 105-108, p. 69-85, and Mosier et al., 2005, Bioresource Technology 96: 673-686, and U.S. Published Application 2002/0164730.

In one aspect, the chemical pretreatment is preferably carried out as a dilute acid treatment, and more preferably as a continuous dilute acid treatment. The acid is typically sulfuric acid, but other acids can also be used, such as acetic acid, citric acid, nitric acid, phosphoric acid, tartaric acid, succinic acid, hydrogen chloride, or mixtures thereof. Mild acid treatment is conducted in the pH range of preferably 1-5, e.g., 1-4 or 1-2.5. In one aspect, the acid concentration is in the range from preferably 0.01 to 10 wt % acid, e.g., 0.05 to 5 wt % acid or 0.1 to 2 wt % acid. The acid is contacted with the cellulosic material and held at a temperature in the range of preferably 140-200° C., e.g., 165-190° C., for periods ranging from 1 to 60 minutes.

In another aspect, pretreatment takes place in an aqueous slurry. In preferred aspects, the cellulosic material is present during pretreatment in amounts preferably between 10-80 wt %, e.g., 20-70 wt % or 30-60 wt %, such as around 40 wt %. The pretreated cellulosic material can be unwashed or washed using any method known in the art, e.g., washed with water.

Mechanical Pretreatment or Physical Pretreatment: The term “mechanical pretreatment” or “physical pretreatment” refers to any pretreatment that promotes size reduction of particles. For example, such pretreatment can involve various types of grinding or milling (e.g., dry milling, wet milling, or vibratory ball milling).

The cellulosic material can be pretreated both physically (mechanically) and chemically. Mechanical or physical pretreatment can be coupled with steaming/steam explosion, hydrothermolysis, dilute or mild acid treatment, high temperature, high pressure treatment, irradiation (e.g., microwave irradiation), or combinations thereof. In one aspect, high pressure means pressure in the range of preferably about 100 to about 400 psi, e.g., about 150 to about 250 psi. In another aspect, high temperature means temperatures in the range of about 100 to about 300° C., e.g., about 140 to about 200° C. In a preferred aspect, mechanical or physical pretreatment is performed in a batch-process using a steam gun hydrolyzer system that uses high pressure and high temperature as defined above, e.g., a Sunds Hydrolyzer available from Sunds Defibrator AB, Sweden. The physical and chemical pretreatments can be carried out sequentially or simultaneously, as desired.

Accordingly, in a preferred aspect, the cellulosic material is subjected to physical (mechanical) or chemical pretreatment, or any combination thereof, to promote the separation and/or release of cellulose, hemicellulose, and/or lignin.

Biological Pretreatment: The term “biological pretreatment” refers to any biological pretreatment that promotes the separation and/or release of cellulose, hemicellulose, and/or lignin from the cellulosic material. Biological pretreatment techniques can involve applying lignin-solubilizing microorganisms and/or enzymes (see, for example, Hsu, T.-A., 1996, Pretreatment of biomass, in Handbook on Bioethanol: Production and Utilization, Wyman, C. E., ed., Taylor & Francis, Washington, D.C., 179-212; Ghosh and Singh, 1993, Physicochemical and biological treatments for enzymatic/microbial conversion of cellulosic biomass, Adv. Appl. Microbiol. 39: 295-333; McMillan, J. D., 1994, Pretreating lignocellulosic biomass: a review, in Enzymatic Conversion of Biomass for Fuels Production, Himmel, M. E., Baker, J. O., and Overend, R. P., eds., ACS Symposium Series 566, American Chemical Society, Washington, D.C., chapter 15; Gong, C. S., Cao, N. J., Du, J., and Tsao, G. T., 1999, Ethanol production from renewable resources, in Advances in Biochemical Engineering/Biotechnology, Scheper, T., ed., Springer-Verlag Berlin Heidelberg, Germany, 65: 207-241; Olsson and Hahn-Hagerdal, 1996, Fermentation of lignocellulosic hydrolysates for ethanol production, Enz. Microb. Tech. 18: 312-331; and Vallander and Eriksson, 1990, Production of ethanol from lignocellulosic materials: State of the art, Adv. Biochem. Eng./Biotechnol. 42: 63-95).

Saccharification.

In the hydrolysis step, also known as saccharification, the cellulosic material, e.g., pretreated, is hydrolyzed to break down cellulose and/or hemicellulose to fermentable sugars, such as glucose, cellobiose, xylose, xylulose, arabinose, mannose, galactose, and/or soluble oligosaccharides. The hydrolysis is performed enzymatically by an enzyme composition as described herein in the presence of a chimeric GH61 polypeptide of the present invention. The enzymes of the compositions can be added simultaneously or sequentially.

Enzymatic hydrolysis is preferably carried out in a suitable aqueous environment under conditions that can be readily determined by one skilled in the art. In one aspect, hydrolysis is performed under conditions suitable for the activity of the enzyme(s), i.e., optimal for the enzyme(s). The hydrolysis can be carried out as a fed batch or continuous process where the cellulosic material is fed gradually to, for example, an enzyme containing hydrolysis solution.

The saccharification is generally performed in stirred-tank reactors or fermentors under controlled pH, temperature, and mixing conditions. Suitable process time, temperature and pH conditions can readily be determined by one skilled in the art. For example, the saccharification can last up to 200 hours, but is typically performed for preferably about 12 to about 120 hours, e.g., about 16 to about 72 hours or about 24 to about 48 hours. The temperature is in the range of preferably about 25° C. to about 70° C., e.g., about 30° C. to about 65° C., about 40° C. to about 60° C., or about 50° C. to about 55° C. The pH is in the range of preferably about 3 to about 8, e.g., about 3.5 to about 7, about 4 to about 6, or about 5.0 to about 5.5. The dry solids content is in the range of preferably about 5 to about 50 wt %, e.g., about 10 to about 40 wt % or about 20 to about 30 wt %.

The enzyme compositions can comprise any protein useful in degrading the cellulosic material.

In one aspect, the enzyme composition comprises or further comprises one or more (e.g., several) proteins selected from the group consisting of a cellulase, a polypeptide having cellulolytic enhancing activity, a hemicellulase, an esterase, an expansin, a laccase, a ligninolytic enzyme, a pectinase, a peroxidase, a protease, and a swollenin. In another aspect, the cellulase is preferably one or more (e.g., several) enzymes selected from the group consisting of an endoglucanase, a cellobiohydrolase, and a beta-glucosidase. In another aspect, the hemicellulase is preferably one or more (e.g., several) enzymes selected from the group consisting of an acetylmannan esterase, an acetylxylan esterase, an arabinanase, an arabinofuranosidase, a coumaric acid esterase, a feruloyl esterase, a galactosidase, a glucuronidase, a glucuronoyl esterase, a mannanase, a mannosidase, a xylanase, and a xylosidase.

In another aspect, the enzyme composition comprises one or more (e.g., several) cellulolytic enzymes. In another aspect, the enzyme composition comprises or further comprises one or more (e.g., several) hemicellulolytic enzymes. In another aspect, the enzyme composition comprises one or more (e.g., several) cellulolytic enzymes and one or more (e.g., several) hemicellulolytic enzymes. In another aspect, the enzyme composition comprises one or more (e.g., several) enzymes selected from the group of cellulolytic enzymes and hemicellulolytic enzymes. In another aspect, the enzyme composition comprises an endoglucanase. In another aspect, the enzyme composition comprises a cellobiohydrolase. In another aspect, the enzyme composition comprises a beta-glucosidase. In another aspect, the enzyme composition comprises a polypeptide having cellulolytic enhancing activity. In another aspect, the enzyme composition comprises an endoglucanase and a polypeptide having cellulolytic enhancing activity. In another aspect, the enzyme composition comprises a cellobiohydrolase and a polypeptide having cellulolytic enhancing activity. In another aspect, the enzyme composition comprises a beta-glucosidase and a polypeptide having cellulolytic enhancing activity. In another aspect, the enzyme composition comprises an endoglucanase and a cellobiohydrolase. In another aspect, the enzyme composition comprises an endoglucanase and a beta-glucosidase. In another aspect, the enzyme composition comprises a cellobiohydrolase and a beta-glucosidase. In another aspect, the enzyme composition comprises an endoglucanase, a cellobiohydrolase, and a polypeptide having cellulolytic enhancing activity. In another aspect, the enzyme composition comprises an endoglucanase, a beta-glucosidase, and a polypeptide having cellulolytic enhancing activity. In another aspect, the enzyme composition comprises a cellobiohydrolase, a beta-glucosidase, and a polypeptide having cellulolytic enhancing activity. In another aspect, the enzyme composition comprises an endoglucanase, a cellobiohydrolase, and a beta-glucosidase. In another aspect, the enzyme composition comprises an endoglucanase, a cellobiohydrolase, a beta-glucosidase, and a polypeptide having cellulolytic enhancing activity.

In another aspect, the enzyme composition comprises an acetylmannan esterase. In another aspect, the enzyme composition comprises an acetylxylan esterase. In another aspect, the enzyme composition comprises an arabinanase (e.g., alpha-L-arabinanase). In another aspect, the enzyme composition comprises an arabinofuranosidase (e.g., alpha-L-arabinofuranosidase). In another aspect, the enzyme composition comprises a coumaric acid esterase. In another aspect, the enzyme composition comprises a feruloyl esterase. In another aspect, the enzyme composition comprises a galactosidase (e.g., alpha-galactosidase and/or beta-galactosidase). In another aspect, the enzyme composition comprises a glucuronidase (e.g., alpha-D-glucuronidase). In another aspect, the enzyme composition comprises a glucuronoyl esterase. In another aspect, the enzyme composition comprises a mannanase. In another aspect, the enzyme composition comprises a mannosidase (e.g., beta-mannosidase). In another aspect, the enzyme composition comprises a xylanase. In a preferred aspect, the xylanase is a Family 10 xylanase. In another aspect, the enzyme composition comprises a xylosidase (e.g., beta-xylosidase).

In another aspect, the enzyme composition comprises an esterase. In another aspect, the enzyme composition comprises an expansin. In another aspect, the enzyme composition comprises a laccase. In another aspect, the enzyme composition comprises a ligninolytic enzyme. In a preferred aspect, the ligninolytic enzyme is a manganese peroxidase. In another preferred aspect, the ligninolytic enzyme is a lignin peroxidase. In another preferred aspect, the ligninolytic enzyme is a H₂O₂-producing enzyme. In another aspect, the enzyme composition comprises a pectinase. In another aspect, the enzyme composition comprises a peroxidase. In another aspect, the enzyme composition comprises a protease. In another aspect, the enzyme composition comprises a swollenin

In the methods of the present invention, the enzyme(s) can be added prior to or during saccharification, saccharification and fermentation, or fermentation.

One or more (e.g., several) components of the enzyme composition may be wild-type proteins, recombinant proteins, or a combination of wild-type proteins and recombinant proteins. For example, one or more (e.g., several) components may be native proteins of a cell, which is used as a host cell to express recombinantly one or more (e.g., several) other components of the enzyme composition. One or more (e.g., several) components of the enzyme composition may be produced as monocomponents, which are then combined to form the enzyme composition. The enzyme composition may be a combination of multicomponent and monocomponent protein preparations.

The enzymes used in the methods of the present invention may be in any form suitable for use, such as, for example, a fermentation broth formulation or a cell composition, a cell lysate with or without cellular debris, a semi-purified or purified enzyme preparation, or a host cell as a source of the enzymes. The enzyme composition may be a dry powder or granulate, a non-dusting granulate, a liquid, a stabilized liquid, or a stabilized protected enzyme. Liquid enzyme preparations may, for instance, be stabilized by adding stabilizers such as a sugar, a sugar alcohol or another polyol, and/or lactic acid or another organic acid according to established processes.

The optimum amounts of the enzymes and chimeric GH61 polypeptides depend on several factors including, but not limited to, the mixture of component cellulolytic and/or hemicellulolytic enzymes, the cellulosic material, the concentration of cellulosic material, the pretreatment(s) of the cellulosic material, temperature, time, pH, and inclusion of fermenting organism (e.g., yeast for Simultaneous Saccharification and Fermentation).

In one aspect, an effective amount of cellulolytic or hemicellulolytic enzyme to the cellulosic material is about 0.5 to about 50 mg, e.g., about 0.5 to about 40 mg, about 0.5 to about 25 mg, about 0.75 to about 20 mg, about 0.75 to about 15 mg, about 0.5 to about 10 mg, or about 2.5 to about 10 mg per g of the cellulosic material.

In another aspect, an effective amount of a chimeric GH61 polypeptide having cellulolytic enhancing activity to the cellulosic material is about 0.01 to about 50.0 mg, e.g., about 0.01 to about 40 mg, about 0.01 to about 30 mg, about 0.01 to about 20 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.025 to about 1.5 mg, about 0.05 to about 1.25 mg, about 0.075 to about 1.25 mg, about 0.1 to about 1.25 mg, about 0.15 to about 1.25 mg, or about 0.25 to about 1.0 mg per g of the cellulosic material.

In another aspect, an effective amount of a chimeric GH61 polypeptide having cellulolytic enhancing activity to cellulolytic or hemicellulolytic enzyme is about 0.005 to about 1.0 g, e.g., about 0.01 to about 1.0 g, about 0.15 to about 0.75 g, about 0.15 to about 0.5 g, about 0.1 to about 0.5 g, about 0.1 to about 0.25 g, or about 0.05 to about 0.2 g per g of cellulolytic or hemicellulolytic enzyme.

The polypeptides having cellulolytic enzyme activity or hemicellulolytic enzyme activity as well as other proteins/polypeptides useful in the degradation of the cellulosic material, e.g., GH61 polypeptides having cellulolytic enhancing activity (collectively hereinafter “polypeptides having enzyme activity”) can be derived or obtained from any suitable origin, including, bacterial, fungal, yeast, plant, or mammalian origin. The term “obtained” also means herein that the enzyme may have been produced recombinantly in a host organism employing methods described herein, wherein the recombinantly produced enzyme is either native or foreign to the host organism or has a modified amino acid sequence, e.g., having one or more (e.g., several) amino acids that are deleted, inserted and/or substituted, i.e., a recombinantly produced enzyme that is a mutant and/or a fragment of a native amino acid sequence or an enzyme produced by nucleic acid shuffling processes known in the art. Encompassed within the meaning of a native enzyme are natural variants and within the meaning of a foreign enzyme are variants obtained recombinantly, such as by site-directed mutagenesis or shuffling.

A polypeptide having enzyme activity may be a bacterial polypeptide. For example, the polypeptide may be a gram positive bacterial polypeptide such as a Bacillus, Streptococcus, Streptomyces, Staphylococcus, Enterococcus, Lactobacillus, Lactococcus, Clostridium, Geobacillus, Caldicellulosiruptor, Acidothermus, Thermobifidia, or Oceanobacillus polypeptide having enzyme activity, or a Gram negative bacterial polypeptide such as an E. coli, Pseudomonas, Salmonella, Campylobacter, Helicobacter, Flavobacterium, Fusobacterium, Ilyobacter, Neisseria, or Ureaplasma polypeptide having enzyme activity.

In one aspect, the polypeptide is a Bacillus alkalophilus, Bacillus amyloliquefaciens, Bacillus brevis, Bacillus circulans, Bacillus clausii, Bacillus coagulans, Bacillus firmus, Bacillus lautus, Bacillus lentus, Bacillus licheniformis, Bacillus megaterium, Bacillus pumilus, Bacillus stearothermophilus, Bacillus subtilis, or Bacillus thuringiensis polypeptide having enzyme activity.

In another aspect, the polypeptide is a Streptococcus equisimilis, Streptococcus pyogenes, Streptococcus uberis, or Streptococcus equi subsp. Zooepidemicus polypeptide having enzyme activity.

In another aspect, the polypeptide is a Streptomyces achromogenes, Streptomyces avermitilis, Streptomyces coelicolor, Streptomyces griseus, or Streptomyces lividans polypeptide having enzyme activity.

The polypeptide having enzyme activity may also be a fungal polypeptide, and more preferably a yeast polypeptide such as a Candida, Kluyveromyces, Pichia, Saccharomyces, Schizosaccharomyces, or Yarrowia polypeptide having enzyme activity; or more preferably a filamentous fungal polypeptide such as an Acremonium, Agaricus, Alternaria, Aspergillus, Aureobasidium, Botryospaeria, Ceriporiopsis, Chaetomidium, Chrysosporium, Claviceps, Cochliobolus, Coprinopsis, Coptotermes, Corynascus, Cryphonectria, Cryptococcus, Diplodia, Exidia, Filibasidium, Fusarium, Gibberella, Holomastigotoides, Humicola, Irpex, Lentinula, Leptospaeria, Magnaporthe, Melanocarpus, Meripilus, Mucor, Myceliophthora, Neocallimastix, Neurospora, Paecilomyces, Penicillium, Phanerochaete, Piromyces, Poitrasia, Pseudoplectania, Pseudotrichonympha, Rhizomucor, Schizophyllum, Scytalidium, Talaromyces, Thermoascus, Thielavia, Tolypocladium, Trichoderma, Trichophaea, Verticillium, Volvariella, or Xylaria polypeptide having enzyme activity.

In one aspect, the polypeptide is a Saccharomyces carlsbergensis, Saccharomyces cerevisiae, Saccharomyces diastaticus, Saccharomyces douglasii, Saccharomyces kluyveri, Saccharomyces norbensis, or Saccharomyces oviformis polypeptide having enzyme activity.

In another aspect, the polypeptide is an Acremonium cellulolyticus, Aspergillus aculeatus, Aspergillus awamori, Aspergillus fumigatus, Aspergillus foetidus, Aspergillus japonicus, Aspergillus nidulans, Aspergillus niger, Aspergillus oryzae, Chrysosporium keratinophilum, Chrysosporium lucknowense, Chrysosporium tropicum, Chrysosporium merdarium, Chrysosporium inops, Chrysosporium pannicola, Chrysosporium queenslandicum, Chrysosporium zonatum, Fusarium bactridioides, Fusarium cerealis, Fusarium crookwellense, Fusarium culmorum, Fusarium graminearum, Fusarium graminum, Fusarium heterosporum, Fusarium negundi, Fusarium oxysporum, Fusarium reticulatum, Fusarium roseum, Fusarium sambucinum, Fusarium sarcochroum, Fusarium sporotrichioides, Fusarium sulphureum, Fusarium torulosum, Fusarium trichothecioides, Fusarium venenatum, Humicola grisea, Humicola insolens, Humicola lanuginosa, Irpex lacteus, Mucor miehei, Myceliophthora thermophila, Neurospora crassa, Penicillium funiculosum, Penicillium purpurogenum, Phanerochaete chrysosporium, Thielavia achromatica, Thielavia albomyces, Thielavia albopilosa, Thielavia australeinsis, Thielavia fimeti, Thielavia microspora, Thielavia ovispora, Thielavia peruviana, Thielavia spededonium, Thielavia setosa, Thielavia subthermophila, Thielavia terrestris, Trichoderma harzianum, Trichoderma koningii, Trichoderma longibrachiatum, Trichoderma reesei, Trichoderma viride, or Trichophaea saccata polypeptide having enzyme activity.

Chemically modified or protein engineered mutants of polypeptides having enzyme activity may also be used.

One or more (e.g., several) components of the enzyme composition may be a recombinant component, i.e., produced by cloning of a DNA sequence encoding the single component and subsequent cell transformed with the DNA sequence and expressed in a host (see, for example, WO 91/17243 and WO 91/17244). The host is preferably a heterologous host (enzyme is foreign to host), but the host may under certain conditions also be a homologous host (enzyme is native to host). Monocomponent cellulolytic proteins may also be prepared by purifying such a protein from a fermentation broth.

In one aspect, the one or more (e.g., several) cellulolytic enzymes comprise a commercial cellulolytic enzyme preparation. Examples of commercial cellulolytic enzyme preparations suitable for use in the present invention include, for example, CELLIC® CTec (Novozymes A/S), CELLIC® CTec2 (Novozymes A/S), CELLUCLAST™ (Novozymes A/S), NOVOZYM™ 188 (Novozymes A/S), CELLUZYME™ (Novozymes A/S), CEREFLO™ (Novozymes A/S), and ULTRAFLO™ (Novozymes A/S), ACCELERASE™ (Genencor Int.), LAMINEX™ (Genencor Int.), SPEZYME™ CP (Genencor Int.), FILTRASE® NL (DSM); METHAPLUS® S/L 100 (DSM), ROHAMENT™ 7069 W (Röhm GmbH), FIBREZYME® LDI (Dyadic International, Inc.), FIBREZYME® LBR (Dyadic International, Inc.), or VISCOSTAR® 150L (Dyadic International, Inc.). The cellulase enzymes are added in amounts effective from about 0.001 to about 5.0 wt % of solids, e.g., about 0.025 to about 4.0 wt % of solids or about 0.005 to about 2.0 wt % of solids.

Examples of bacterial endoglucanases that can be used in the methods of the present invention, include, but are not limited to, an Acidothermus cellulolyticus endoglucanase (WO 91/05039; WO 93/15186; U.S. Pat. No. 5,275,944; WO 96/02551; U.S. Pat. No. 5,536,655, WO 00/70031, WO 05/093050); Thermobifida fusca endoglucanase III (WO 05/093050); and Thermobifida fusca endoglucanase V (WO 05/093050).

Examples of fungal endoglucanases that can be used in the present invention include, but are not limited to, a Trichoderma reesei endoglucanase I (Penttila et al., 1986, Gene 45: 253-263; Trichoderma reesei Cel7B endoglucanase I; GENBANK™ accession no. M15665; SEQ ID NO: 2); Trichoderma reesei endoglucanase II (Saloheimo, et al., 1988, Gene 63:11-22; Trichoderma reesei Cel5A endoglucanase II; GENBANK™ accession no. M19373; SEQ ID NO: 4); Trichoderma reesei endoglucanase III (Okada et al., 1988, Appl. Environ. Microbiol. 64: 555-563; GENBANK™ accession no. AB003694; SEQ ID NO: 6); Trichoderma reesei endoglucanase V (Saloheimo et al., 1994, Molecular Microbiology 13: 219-228; GENBANK™ accession no. Z33381; SEQ ID NO: 8); Aspergillus aculeatus endoglucanase (Ooi et al., 1990, Nucleic Acids Research 18: 5884); Aspergillus kawachii endoglucanase (Sakamoto et al., 1995, Current Genetics 27: 435-439); Erwinia carotovara endoglucanase (Saarilahti et al., 1990, Gene 90: 9-14); Fusarium oxysporum endoglucanase (GENBANK™ accession no. L29381); Humicola grisea var. thermoidea endoglucanase (GENBANK™ accession no. AB003107); Melanocarpus albomyces endoglucanase (GENBANK™ accession no. MAL515703); Neurospora crassa endoglucanase (GENBANK™ accession no. XM_(—)324477); Humicola insolens endoglucanase V (SEQ ID NO: 10); Myceliophthora thermophila CBS 117.65 endoglucanase (SEQ ID NO: 12); basidiomycete CBS 495.95 endoglucanase (SEQ ID NO: 14); basidiomycete CBS 494.95 endoglucanase (SEQ ID NO: 16); Thielavia terrestris NRRL 8126 CEL6B endoglucanase (SEQ ID NO: 18); Thielavia terrestris NRRL 8126 CEL6C endoglucanase (SEQ ID NO: 20); Thielavia terrestris NRRL 8126 CEL7C endoglucanase (SEQ ID NO: 22); Thielavia terrestris NRRL 8126 CEL7E endoglucanase (SEQ ID NO: 24); Thielavia terrestris NRRL 8126 CEL7F endoglucanase (SEQ ID NO: 26); Cladorrhinum foecundissimum ATCC 62373 CEL7A endoglucanase (SEQ ID NO: 28); and Trichoderma reesei strain No. VTT-D-80133 endoglucanase (SEQ ID NO: 30; GENBANK™ accession no. M15665). The endoglucanases of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, and SEQ ID NO: 30, described above are encoded by the mature polypeptide coding sequence of SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21, SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, and SEQ ID NO: 29, respectively.

Examples of cellobiohydrolases useful in the present invention include, but are not limited to, Trichoderma reesei cellobiohydrolase I (SEQ ID NO: 32); Trichoderma reesei cellobiohydrolase II (SEQ ID NO: 34); Humicola insolens cellobiohydrolase I (SEQ ID NO: 36); Myceliophthora thermophila cellobiohydrolase II (SEQ ID NO: 38 and SEQ ID NO: 40); Thielavia terrestris cellobiohydrolase II (CEL6A) (SEQ ID NO: 42); Chaetomium thermophilum cellobiohydrolase I (SEQ ID NO: 44); and Chaetomium thermophilum cellobiohydrolase II (SEQ ID NO: 46), Aspergillus fumigatus cellobiohydrolase I (SEQ ID NO: 48), and Aspergillus fumigatus cellobiohydrolase II (SEQ ID NO: 50). The cellobiohydrolases of SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, and SEQ ID NO: 50, described above are encoded by the mature polypeptide coding sequence of SEQ ID NO: 31, SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37, SEQ ID NO: 39, SEQ ID NO: 41, SEQ ID NO: 43, SEQ ID NO: 45, SEQ ID NO: 47, and SEQ ID NO: 49, respectively.

Examples of beta-glucosidases useful in the present invention include, but are not limited to, Aspergillus oryzae beta-glucosidase (SEQ ID NO: 52); Aspergillus fumigatus beta-glucosidase (SEQ ID NO: 54); Penicillium brasilianum IBT 20888 beta-glucosidase (SEQ ID NO: 56); Aspergillus niger beta-glucosidase (SEQ ID NO: 58); and Aspergillus aculeatus beta-glucosidase (SEQ ID NO: 60). The beta-glucosidases of SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, and SEQ ID NO: 60, described above are encoded by the mature polypeptide coding sequence of SEQ ID NO: 51, SEQ ID NO: 53, SEQ ID NO: 55, SEQ ID NO: 57, and SEQ ID NO: 59, respectively.

Examples of other beta-glucosidases useful in the present invention include a Aspergillus oryzae beta-glucosidase variant fusion protein of SEQ ID NO: 62 or the Aspergillus oryzae beta-glucosidase fusion protein of SEQ ID NO: 64. The beta-glucosidase fusion proteins of SEQ ID NO: 62 and SEQ ID NO: 64 are encoded by SEQ ID NO: 61 and SEQ ID NO: 63, respectively.

Other useful endoglucanases, cellobiohydrolases, and beta-glucosidases are disclosed in numerous Glycosyl Hydrolase families using the classification according to Henrissat B., 1991, A classification of glycosyl hydrolases based on amino-acid sequence similarities, Biochem. J. 280: 309-316, and Henrissat B., and Bairoch A., 1996, Updating the sequence-based classification of glycosyl hydrolases, Biochem. J. 316: 695-696.

Other cellulolytic enzymes that may be used in the present invention are described in WO 98/13465, WO 98/015619, WO 98/015633, WO 99/06574, WO 99/10481, WO 99/025847, WO 99/031255, WO 2002/101078, WO 2003/027306, WO 2003/052054, WO 2003/052055, WO 2003/052056, WO 2003/052057, WO 2003/052118, WO 2004/016760, WO 2004/043980, WO 2004/048592, WO 2005/001065, WO 2005/028636, WO 2005/093050, WO 2005/093073, WO 2006/074005, WO 2006/117432, WO 2007/071818, WO 2007/071820, WO 2008/008070, WO 2008/008793, U.S. Pat. No. 5,457,046, U.S. Pat. No. 5,648,263, and U.S. Pat. No. 5,686,593.

In the methods of the present invention, any GH61 polypeptide having cellulolytic enhancing activity can be used as a component of the enzyme composition.

Examples of GH61 polypeptides having cellulolytic enhancing activity useful in the processes of the present invention include, but are not limited to, GH61 polypeptides from Thielavia terrestris (WO 2005/074647, WO 2008/148131, and WO 2011/035027), Thermoascus aurantiacus (WO 2005/074656 and WO 2010/065830), Trichoderma reesei (WO 2007/089290), Myceliophthora thermophila (WO 2009/085935, WO 2009/085859, WO 2009/085864, WO 2009/085868), Aspergillus fumigatus (WO 2010/138754), GH61 polypeptides from Penicillium pinophilum (WO 2011/005867), Thermoascus sp. (WO 2011/039319), Penicillium sp. (WO 2011/041397), and Thermoascus crustaceous (WO 2011/041504).

In a first aspect, the GH61 polypeptide having cellulolytic enhancing activity comprises the following motifs:

(SEQ ID NO: 171 or SEQ ID NO: 172) [ILMV]-P-X(4,5)-G-X-Y-[ILMV]-X-R-X-[EQ]-X(4)-[HNQ] and [FW]-[TF]-K-[AIV], wherein X is any amino acid, X(4,5) is any amino acid at 4 or 5 contiguous positions, and X(4) is any amino acid at 4 contiguous positions.

The isolated polypeptide comprising the above-noted motifs may further comprise:

(SEQ ID NO: 173 or SEQ ID NO: 174) H-X(1,2)-G-P-X(3)-[YW]-[AILMV], (SEQ ID NO: 175) [EQ]-X-Y-X(2)-C-X-[EHQN]-[FILV]-X-[ILV], or (SEQ ID NO: 176 or SEQ ID NO: 177) H-X(1,2)-G-P-X(3)-[YW]-[AILMV] and (SEQ ID NO: 178) [EQ]-X-Y-X(2)-C-X-[EHQN]-[FILV]-X-[ILV], wherein X is any amino acid, X(1,2) is any amino acid at 1 position or 2 contiguous positions, X(3) is any amino acid at 3 contiguous positions, and X(2) is any amino acid at 2 contiguous positions. In the above motifs, the accepted IUPAC single letter amino acid abbreviation is employed.

In a preferred embodiment, the isolated GH61 polypeptide having cellulolytic enhancing activity further comprises H-X(1,2)-G-P-X(3)-[YW]-[AILMV] (SEQ ID NO: 179 or SEQ ID NO: 180). In another preferred embodiment, the isolated GH61 polypeptide having cellulolytic enhancing activity further comprises [EQ]X-Y-X(2)-C-X-[EHQN]-[FILV]X-[ILV] (SEQ ID NO: 181). In another preferred embodiment, the isolated GH61 polypeptide having cellulolytic enhancing activity further comprises H-X(1,2)-G-P-X(3)-[YW]-[AILMV] (SEQ ID NO: 182 or SEQ ID NO: 183) and [EQ]-X-Y-X(2)-C-X-[EHQN]-[FILV]-X-[ILV] (SEQ ID NO: 184).

In a second aspect, isolated polypeptides having cellulolytic enhancing activity, comprise the following motif:

(SEQ ID NO: 185 or SEQ ID NO: 186) [ILMV]-P-X(4,5)-G-X-Y-[ILMV]-X-R-X-[EQ]-X(3)-A- [HNQ], wherein X is any amino acid, X(4,5) is any amino acid at 4 or 5 contiguous positions, and X(3) is any amino acid at 3 contiguous positions. In the above motif, the accepted IUPAC single letter amino acid abbreviation is employed.

In a third aspect, the polypeptide having cellulolytic enhancing activity comprises an amino acid sequence that has a sequence identity to the mature polypeptide of SEQ ID NO: 66, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 72, SEQ ID NO: 74, SEQ ID NO: 76, SEQ ID NO: 78, SEQ ID NO: 80, SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90, SEQ ID NO: 92, SEQ ID NO: 94, SEQ ID NO: 96, SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 110, SEQ ID NO: 112, SEQ ID NO: 114, SEQ ID NO: 116, SEQ ID NO: 118, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 144, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 166, SEQ ID NO: 168, or SEQ ID NO: 170 of at least 60%, e.g., at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, or at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or at least 100%.

In a fourth aspect, the polypeptide having cellulolytic enhancing activity is encoded by a polynucleotide that hybridizes under at least very low stringency conditions, preferably at least low stringency conditions, more preferably at least medium stringency conditions, more preferably at least medium-high stringency conditions, even more preferably at least high stringency conditions, and most preferably at least very high stringency conditions with (i) the mature polypeptide coding sequence of SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 71, SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 77, SEQ ID NO: 79, SEQ ID NO: 81, SEQ ID NO: 83, SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91, SEQ ID NO: 93, SEQ ID NO: 95, SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101, SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, SEQ ID NO: 111, SEQ ID NO: 113, SEQ ID NO: 115, SEQ ID NO: 117, SEQ ID NO: 119, SEQ ID NO: 121, SEQ ID NO: 123, SEQ ID NO: 125, SEQ ID NO: 127, SEQ ID NO: 143, SEQ ID NO: 145, SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 151, SEQ ID NO: 153, SEQ ID NO: 155, SEQ ID NO: 157, SEQ ID NO: 159, SEQ ID NO: 161, SEQ ID NO: 163, SEQ ID NO: 165, SEQ ID NO: 167, or SEQ ID NO: 169, (ii) the cDNA sequence of the mature polypeptide coding sequence of SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 77, SEQ ID NO: 81, SEQ ID NO: 83, SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91, SEQ ID NO: 93, SEQ ID NO: 95, SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101, SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, SEQ ID NO: 111, SEQ ID NO: 113, SEQ ID NO: 115, SEQ ID NO: 117, SEQ ID NO: 119, SEQ ID NO: 121, SEQ ID NO: 123, SEQ ID NO: 125, or SEQ ID NO: 127, SEQ ID NO: 143, SEQ ID NO: 145, SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 151, SEQ ID NO: 153, SEQ ID NO: 155, SEQ ID NO: 157, SEQ ID NO: 159, SEQ ID NO: 167, or SEQ ID NO: 169, or the genomic DNA sequence comprising the mature polypeptide coding sequence of SEQ ID NO: 71, SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 79, SEQ ID NO: 161, SEQ ID NO: 163, or SEQ ID NO: 165, (iii) a subsequence of (i) or (ii), or (iv) a full-length complement of (i), (ii), or (iii) (J. Sambrook, E. F. Fritsch, and T. Maniatus, 1989, supra). A subsequence of the mature polypeptide coding sequence of SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 71, SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 77, SEQ ID NO: 79, SEQ ID NO: 81, SEQ ID NO: 83, SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91, SEQ ID NO: 93, SEQ ID NO: 95, SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101, SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, SEQ ID NO: 111, SEQ ID NO: 113, SEQ ID NO: 115, SEQ ID NO: 117, SEQ ID NO: 119, SEQ ID NO: 121, SEQ ID NO: 123, SEQ ID NO: 125, SEQ ID NO: 127, SEQ ID NO: 143, SEQ ID NO: 145, SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 151, SEQ ID NO: 153, SEQ ID NO: 155, SEQ ID NO: 157, SEQ ID NO: 159, SEQ ID NO: 161, SEQ ID NO: 163, SEQ ID NO: 165, SEQ ID NO: 167, or SEQ ID NO: 169 contains at least 100 contiguous nucleotides or preferably at least 200 contiguous nucleotides. Moreover, the subsequence may encode a polypeptide fragment that has cellulolytic enhancing activity.

In a fifth aspect, the polypeptide having cellulolytic enhancing activity is encoded by a polynucleotide comprising or consisting of a nucleotide sequence that has a sequence identity to the mature polypeptide coding sequence of SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 71, SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 77, SEQ ID NO: 79, SEQ ID NO: 81, SEQ ID NO: 83, SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91, SEQ ID NO: 93, SEQ ID NO: 95, SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101, SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, SEQ ID NO: 111, SEQ ID NO: 113, SEQ ID NO: 115, SEQ ID NO: 117, SEQ ID NO: 119, SEQ ID NO: 121, SEQ ID NO: 123, SEQ ID NO: 125, SEQ ID NO: 127, SEQ ID NO: 143, SEQ ID NO: 145, SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 151, SEQ ID NO: 153, SEQ ID NO: 155, SEQ ID NO: 157, SEQ ID NO: 159, SEQ ID NO: 161, SEQ ID NO: 163, SEQ ID NO: 165, SEQ ID NO: 167, or SEQ ID NO: 169, or the cDNA sequence of the mature polypeptide coding sequence of SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 77, SEQ ID NO: 81, SEQ ID NO: 83, SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91, SEQ ID NO: 93, SEQ ID NO: 95, SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101, SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, SEQ ID NO: 111, SEQ ID NO: 113, SEQ ID NO: 115, SEQ ID NO: 117, SEQ ID NO: 119, SEQ ID NO: 121, SEQ ID NO: 123, SEQ ID NO: 125, or SEQ ID NO: 127, SEQ ID NO: 143, SEQ ID NO: 145, SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 151, SEQ ID NO: 153, SEQ ID NO: 155, SEQ ID NO: 157, SEQ ID NO: 159, SEQ ID NO: 167, or SEQ ID NO: 169, or the genomic DNA sequence comprising the mature polypeptide coding sequence of SEQ ID NO: 71, SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 79, SEQ ID NO: 161, SEQ ID NO: 163, or SEQ ID NO: 165, of preferably at least 60%, more preferably at least 65%, more preferably at least 70%, more preferably at least 75%, more preferably at least 80%, more preferably at least 85%, even more preferably at least 90%, most preferably at least 91%, at least 92%, at least 93%, at least 94%, or at least 95%, and even most preferably at least 96%, at least 97%, at least 98%, at least 99%, or at least 100%.

In a sixth aspect, the polypeptide having cellulolytic enhancing activity is an artificial variant comprising a substitution, deletion, and/or insertion of one or more (or several) amino acids of the mature polypeptide of SEQ ID NO: 66, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 72, SEQ ID NO: 74, SEQ ID NO: 76, SEQ ID NO: 78, SEQ ID NO: 80, SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90, SEQ ID NO: 92, SEQ ID NO: 94, SEQ ID NO: 96, SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 110, SEQ ID NO: 112, SEQ ID NO: 114, SEQ ID NO: 116, SEQ ID NO: 118, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 144, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 166, SEQ ID NO: 168, or SEQ ID NO: 170; or a homologous sequence thereof.

Preferably, amino acid changes are of a minor nature, that is conservative amino acid substitutions or insertions that do not significantly affect the folding and/or activity of the protein; small deletions, typically of one to about 30 amino acids; small amino- or carboxyl-terminal extensions, such as an amino-terminal methionine residue; a small linker peptide of up to about 20-25 residues; or a small extension that facilitates purification by changing net charge or another function, such as a poly-histidine tract, an antigenic epitope or a binding domain.

Examples of conservative substitutions are within the group of basic amino acids (arginine, lysine and histidine), acidic amino acids (glutamic acid and aspartic acid), polar amino acids (glutamine and asparagine), hydrophobic amino acids (leucine, isoleucine and valine), aromatic amino acids (phenylalanine, tryptophan and tyrosine), and small amino acids (glycine, alanine, serine, threonine and methionine). Amino acid substitutions that do not generally alter specific activity are known in the art and are described, for example, by H. Neurath and R. L. Hill, 1979, In, The Proteins, Academic Press, New York. The most commonly occurring exchanges are Ala/Ser, Val/Ile, Asp/Glu, Thr/Ser, Ala/Gly, Ala/Thr, Ser/Asn, Ala/Val, Ser/Gly, Tyr/Phe, Ala/Pro, Lys/Arg, Asp/Asn, Leu/Ile, Leu/Val, Ala/Glu, and Asp/Gly.

Alternatively, the amino acid changes are of such a nature that the physico-chemical properties of the polypeptides are altered. For example, amino acid changes may improve the thermal stability of the polypeptide, alter the substrate specificity, change the pH optimum, and the like.

Essential amino acids in a parent polypeptide can be identified according to procedures known in the art, such as site-directed mutagenesis or alanine-scanning mutagenesis (Cunningham and Wells, 1989, Science 244: 1081-1085). In the latter technique, single alanine mutations are introduced at every residue in the molecule, and the resultant mutant molecules are tested for cellulolytic enhancing activity to identify amino acid residues that are critical to the activity of the molecule. See also, Hilton et al., 1996, J. Biol. Chem. 271: 4699-4708. The active site of the enzyme or other biological interaction can also be determined by physical analysis of structure, as determined by such techniques as nuclear magnetic resonance, crystallography, electron diffraction, or photoaffinity labeling, in conjunction with mutation of putative contact site amino acids. See, for example, de Vos et al., 1992, Science 255: 306-312; Smith et al., 1992, J. Mol. Biol. 224: 899-904; Wlodaver et al., 1992, FEBS Lett. 309: 59-64. The identities of essential amino acids can also be inferred from analysis of identities with polypeptides that are related to the parent polypeptide.

Single or multiple amino acid substitutions, deletions, and/or insertions can be made and tested using known methods of mutagenesis, recombination, and/or shuffling, followed by a relevant screening procedure, such as those disclosed by Reidhaar-Olson and Sauer, 1988, Science 241: 53-57; Bowie and Sauer, 1989, Proc. Natl. Acad. Sci. USA 86: 2152-2156; WO 95/17413; or WO 95/22625. Other methods that can be used include error-prone PCR, phage display (e.g., Lowman et al., 1991, Biochemistry 30: 10832-10837; U.S. Pat. No. 5,223,409; WO 92/06204), and region-directed mutagenesis (Derbyshire et al., 1986, Gene 46: 145; Ner et al., 1988, DNA 7: 127).

Mutagenesis/shuffling methods can be combined with high-throughput, automated screening methods to detect activity of cloned, mutagenized polypeptides expressed by host cells (Ness et al., 1999, Nature Biotechnology 17: 893-896). Mutagenized DNA molecules that encode active polypeptides can be recovered from the host cells and rapidly sequenced using standard methods in the art. These methods allow the rapid determination of the importance of individual amino acid residues in a polypeptide.

The total number of amino acid substitutions, deletions and/or insertions of the mature polypeptide of SEQ ID NO: 66, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 72, SEQ ID NO: 74, SEQ ID NO: 76, SEQ ID NO: 78, SEQ ID NO: 80, SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90, SEQ ID NO: 92, SEQ ID NO: 94, SEQ ID NO: 96, SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 110, SEQ ID NO: 112, SEQ ID NO: 114, SEQ ID NO: 116, SEQ ID NO: 118, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 144, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 166, SEQ ID NO: 168, or SEQ ID NO: 170 is not more than 10, e.g., 1, 2, 3, 4, 5, 6, 7, 8, or 9.

In one aspect, the chimeric GH61 polypeptide and GH61 polypeptide having cellulolytic enhancing activity are used in the presence of a soluble activating divalent metal cation according to WO 2008/151043, e.g., manganese sulfate.

In another aspect, the chimeric GH61 polypeptide and GH61 polypeptide having cellulolytic enhancing activity are used in the presence of a dioxy compound, a bicylic compound, a heterocyclic compound, a nitrogen-containing compound, a quinone compound, a sulfur-containing compound, or a liquor obtained from a pretreated cellulosic material such as pretreated corn stover (PCS).

The dioxy compound may include any suitable compound containing two or more oxygen atoms. In some aspects, the dioxy compounds contain a substituted aryl moiety as described herein. The dioxy compounds may comprise one or more (e.g., several) hydroxyl and/or hydroxyl derivatives, but also include substituted aryl moieties lacking hydroxyl and hydroxyl derivatives. Non-limiting examples of the dioxy compounds include pyrocatechol or catechol; caffeic acid; 3,4-dihydroxybenzoic acid; 4-tert-butyl-5-methoxy-1,2-benzenediol; pyrogallol; gallic acid; methyl-3,4,5-trihydroxybenzoate; 2,3,4-trihydroxybenzophenone; 2,6-dimethoxyphenol; sinapinic acid; 3,5-dihydroxybenzoic acid; 4-chloro-1,2-benzenediol; 4-nitro-1,2-benzenediol; tannic acid; ethyl gallate; methyl glycolate; dihydroxyfumaric acid; 2-butyne-1,4-diol; (croconic acid; 1,3-propanediol; tartaric acid; 2,4-pentanediol; 3-ethyoxy-1,2-propanediol; 2,4,4′-trihydroxybenzophenone; cis-2-butene-1,4-diol; 3,4-dihydroxy-3-cyclobutene-1,2-dione; dihydroxyacetone; acrolein acetal; methyl-4-hydroxybenzoate; 4-hydroxybenzoic acid; and methyl-3,5-dimethoxy-4-hydroxybenzoate; or a salt or solvate thereof.

The bicyclic compound may include any suitable substituted fused ring system as described herein. The compounds may comprise one or more (e.g., several) additional rings, and are not limited to a specific number of rings unless otherwise stated. In one aspect, the bicyclic compound is a flavonoid. In another aspect, the bicyclic compound is an optionally substituted isoflavonoid. In another aspect, the bicyclic compound is an optionally substituted flavylium ion, such as an optionally substituted anthocyanidin or optionally substituted anthocyanin, or derivative thereof. Non-limiting examples of the bicyclic compounds include epicatechin; quercetin; myricetin; taxifolin; kaempferol; morin; acacetin; naringenin; isorhamnetin; apigenin; cyanidin; cyanin; kuromanin; keracyanin; or a salt or solvate thereof.

The heterocyclic compound may be any suitable compound, such as an optionally substituted aromatic or non-aromatic ring comprising a heteroatom, as described herein. In one aspect, the heterocyclic is a compound comprising an optionally substituted heterocycloalkyl moiety or an optionally substituted heteroaryl moiety. In another aspect, the optionally substituted heterocycloalkyl moiety or optionally substituted heteroaryl moiety is an optionally substituted 5-membered heterocycloalkyl or an optionally substituted 5-membered heteroaryl moiety. In another aspect, the optionally substituted heterocycloalkyl or optionally substituted heteroaryl moiety is an optionally substituted moiety selected from pyrazolyl, furanyl, imidazolyl, isoxazolyl, oxadiazolyl, oxazolyl, pyrrolyl, pyridyl, pyrimidyl, pyridazinyl, thiazolyl, triazolyl, thienyl, dihydrothieno-pyrazolyl, thianaphthenyl, carbazolyl, benzimidazolyl, benzothienyl, benzofuranyl, indolyl, quinolinyl, benzotriazolyl, benzothiazolyl, benzooxazolyl, benzimidazolyl, isoquinolinyl, isoindolyl, acridinyl, benzoisazolyl, dimethylhydantoin, pyrazinyl, tetrahydrofuranyl, pyrrolinyl, pyrrolidinyl, morpholinyl, indolyl, diazepinyl, azepinyl, thiepinyl, piperidinyl, and oxepinyl. In another aspect, the optionally substituted heterocycloalkyl moiety or optionally substituted heteroaryl moiety is an optionally substituted furanyl. Non-limiting examples of the heterocyclic compounds include (1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one; 4-hydroxy-5-methyl-3-furanone; 5-hydroxy-2(5H)-furanone; [1,2-dihydroxyethyl]furan-2,3,4(5H)-trione; α-hydroxy-γ-butyrolactone; ribonic γ-lactone; aldohexuronicaldohexuronic acid γ-lactone; gluconic acid δ-lactone; 4-hydroxycoumarin; dihydrobenzofuran; 5-(hydroxymethyl)furfural; furoin; 2(5H)-furanone; 5,6-dihydro-2H-pyran-2-one; and 5,6-dihydro-4-hydroxy-6-methyl-2H-pyran-2-one; or a salt or solvate thereof.

The nitrogen-containing compound may be any suitable compound with one or more nitrogen atoms. In one aspect, the nitrogen-containing compound comprises an amine, imine, hydroxylamine, or nitroxide moiety. Non-limiting examples of the nitrogen-containing compounds include acetone oxime; violuric acid; pyridine-2-aldoxime; 2-aminophenol; 1,2-benzenediamine; 2,2,6,6-tetramethyl-1-piperidinyloxy; 5,6,7,8-tetrahydrobiopterin; 6,7-dimethyl-5,6,7,8-tetrahydropterine; and maleamic acid; or a salt or solvate thereof.

The quinone compound may be any suitable compound comprising a quinone moiety as described herein. Non-limiting examples of the quinone compounds include 1,4-benzoquinone; 1,4-naphthoquinone; 2-hydroxy-1,4-naphthoquinone; 2,3-dimethoxy-5-methyl-1,4-benzoquinone or coenzyme Q₀; 2,3,5,6-tetramethyl-1,4-benzoquinone or duroquinone; 1,4-dihydroxyanthraquinone; 3-hydroxy-1-methyl-5,6-indolinedione or adrenochrome; 4-tert-butyl-5-methoxy-1,2-benzoquinone; pyrroloquinoline quinone; or a salt or solvate thereof.

The sulfur-containing compound may be any suitable compound comprising one or more sulfur atoms. In one aspect, the sulfur-containing comprises a moiety selected from thionyl, thioether, sulfinyl, sulfonyl, sulfamide, sulfonamide, sulfonic acid, and sulfonic ester. Non-limiting examples of the sulfur-containing compounds include ethanethiol; 2-propanethiol; 2-propene-1-thiol; 2-mercaptoethanesulfonic acid; benzenethiol; benzene-1,2-dithiol; cysteine; methionine; glutathione; cystine; or a salt or solvate thereof.

In one aspect, an effective amount of such a compound described above to cellulosic material as a molar ratio to glucosyl units of cellulose is about 10⁻⁶ to about 10, e.g., about 10⁻⁶ to about 7.5, about 10⁻⁶ to about 5, about 10⁻⁶ to about 2.5, about 10⁻⁶ to about 1, about 10⁻⁵ to about 1, about 10⁻⁵ to about 10⁻¹, about 10⁻⁴ to about 10⁻¹, about 10⁻³ to about 10⁻¹, or about 10⁻³ to about 10⁻². In another aspect, an effective amount of such a compound described above is about 0.1 μM to about 1 M, e.g., about 0.5 μM to about 0.75 M, about 0.75 μM to about 0.5 M, about 1 μM to about 0.25 M, about 1 μM to about 0.1 M, about 5 μM to about 50 mM, about 10 μM to about 25 mM, about 50 μM to about 25 mM, about 10 μM to about 10 mM, about 5 μM to about 5 mM, or about 0.1 mM to about 1 mM.

The term “liquor” means the solution phase, either aqueous, organic, or a combination thereof, arising from treatment of a lignocellulose and/or hemicellulose material in a slurry, or monosaccharides thereof, e.g., xylose, arabinose, mannose, etc., under conditions as described herein, and the soluble contents thereof. A liquor for cellulolytic enhancement of a GH61 polypeptide can be produced by treating a lignocellulose or hemicellulose material (or feedstock) by applying heat and/or pressure, optionally in the presence of a catalyst, e.g., acid, optionally in the presence of an organic solvent, and optionally in combination with physical disruption of the material, and then separating the solution from the residual solids. Such conditions determine the degree of cellulolytic enhancement obtainable through the combination of liquor and a GH61 polypeptide during hydrolysis of a cellulosic substrate by a cellulase preparation. The liquor can be separated from the treated material using a method standard in the art, such as filtration, sedimentation, or centrifugation.

In one aspect, an effective amount of the liquor to cellulose is about 10⁻⁶ to about 10 g per g of cellulose, e.g., about 10⁻⁶ to about 7.5 g, about 10⁻⁶ to about 5, about 10⁻⁶ to about 2.5 g, about 10⁻⁶ to about 1 g, about 10⁻⁵ to about 1 g, about 10⁻⁵ to about 10⁻¹ g, about 10⁻⁴ to about 10⁻¹ g, about 10⁻³ to about 10⁻¹ g, or about 10⁻³ to about 10⁻² g per g of cellulose.

In one aspect, the one or more (e.g., several) hemicellulolytic enzymes comprise a commercial hemicellulolytic enzyme preparation. Examples of commercial hemicellulolytic enzyme preparations suitable for use in the present invention include, for example, SHEARZYME™ (Novozymes A/S), CELLIC® HTec (Novozymes A/S), CELLIC® HTec2 (Novozymes A/S), VISCOZYME® (Novozymes A/S), ULTRAFLO® (Novozymes A/S), PULPZYME® HC (Novozymes A/S), MULTIFECT® Xylanase (Genencor), ACCELLERASE® XY (Genencor), ACCELLERASE® XC (Genencor), ECOPULP® TX-200A (AB Enzymes), HSP 6000 Xylanase (DSM), DEPOL™ 333P (Biocatalysts Limit, Wales, UK), DEPOL™ 740L. (Biocatalysts Limit, Wales, UK), and DEPOL™ 762P (Biocatalysts Limit, Wales, UK).

Examples of xylanases useful in the methods of the present invention include, but are not limited to, Aspergillus aculeatus xylanase (GeneSeqP:AAR63790; WO 94/21785), Aspergillus fumigatus xylanases (WO 2006/078256; xyl 3 SEQ ID NO: 129 [DNA sequence] and SEQ ID NO: 130 [deduced amino acid sequence]), and Thielavia terrestris NRRL 8126 xylanases (WO 2009/079210).

Examples of beta-xylosidases useful in the methods of the present invention include, but are not limited to, Trichoderma reesei beta-xylosidase (UniProtKB/TrEMBL accession number Q92458; SEQ ID NO: 131 [DNA sequence] and SEQ ID NO: 132 [deduced amino acid sequence]), Talaromyces emersonii (SwissProt accession number Q8X212), and Neurospora crassa (SwissProt accession number Q7SOW4).

Examples of acetylxylan esterases useful in the methods of the present invention include, but are not limited to, acetylxylan esterases from Aspergillus aculeatus (WO 2010/108918), Chaetomium globosum (Uniprot accession number Q2GWX4), Chaetomium gracile (GeneSeqP accession number AAB82124), Humicola insolens DSM 1800 (WO 2009/073709), Hypocrea jecorina (WO 2005/001036), Myceliophtera thermophila (WO 2010/014880), Neurospora crassa (UniProt accession number q7s259), Phaeosphaeria nodorum (Uniprot accession number Q0UHJ1), and Thielavia terrestris NRRL 8126 (WO 2009/042846).

Examples of feruloyl esterases (ferulic acid esterases) useful in the methods of the present invention include, but are not limited to, feruloyl esterases form Humicola insolens DSM 1800 (WO 2009/076122), Neosartorya fischeri (UniProt Accession number A1D9T4), Neurospora crassa (UniProt accession number Q9HGR3), Penicillium aurantiogriseum (WO 2009/127729), and Thielavia terrestris (WO 2010/053838 and WO 2010/065448).

Examples of arabinofuranosidases useful in the methods of the present invention include, but are not limited to, arabinofuranosidases from Aspergillus niger (GeneSeqP accession number AAR94170), Humicola insolens DSM 1800 (WO 2006/114094 and WO 2009/073383), and M. giganteus (WO 2006/114094).

Examples of alpha-glucuronidases useful in the methods of the present invention include, but are not limited to, alpha-glucuronidases from Aspergillus clavatus (UniProt accession number alcc12), Aspergillus fumigatus (SwissProt accession number Q4WW45), Aspergillus niger (Uniprot accession number Q96WX9), Aspergillus terreus (SwissProt accession number Q0CJP9), Humicola insolens (WO 2010/014706), Penicillium aurantiogriseum (WO 2009/068565), Talaromyces emersonii (UniProt accession number Q8×211), and Trichoderma reesei (Uniprot accession number Q99024).

The polypeptides having enzyme activity used in the methods of the present invention may be produced by fermentation of the above-noted microbial strains on a nutrient medium containing suitable carbon and nitrogen sources and inorganic salts, using procedures known in the art (see, e.g., Bennett, J. W. and LaSure, L. (eds.), More Gene Manipulations in Fungi, Academic Press, CA, 1991). Suitable media are available from commercial suppliers or may be prepared according to published compositions (e.g., in catalogues of the American Type Culture Collection). Temperature ranges and other conditions suitable for growth and enzyme production are known in the art (see, e.g., Bailey, J. E., and 011 is, D. F., Biochemical Engineering Fundamentals, McGraw-Hill Book Company, NY, 1986).

The fermentation can be any method of cultivation of a cell resulting in the expression or isolation of an enzyme or protein. Fermentation may, therefore, be understood as comprising shake flask cultivation, or small- or large-scale fermentation (including continuous, batch, fed-batch, or solid state fermentations) in laboratory or industrial fermentors performed in a suitable medium and under conditions allowing the enzyme to be expressed or isolated. The resulting enzymes produced by the methods described above may be recovered from the fermentation medium and purified by conventional procedures.

Fermentation.

The fermentable sugars obtained from the hydrolyzed cellulosic material can be fermented by one or more (e.g., several) fermenting microorganisms capable of fermenting the sugars directly or indirectly into a desired fermentation product. “Fermentation” or “fermentation process” refers to any fermentation process or any process comprising a fermentation step. Fermentation processes also include fermentation processes used in the consumable alcohol industry (e.g., beer and wine), dairy industry (e.g., fermented dairy products), leather industry, and tobacco industry. The fermentation conditions depend on the desired fermentation product and fermenting organism and can easily be determined by one skilled in the art.

In the fermentation step, sugars, released from the cellulosic material as a result of the pretreatment and enzymatic hydrolysis steps, are fermented to a product, e.g., ethanol, by a fermenting organism, such as yeast. Hydrolysis (saccharification) and fermentation can be separate or simultaneous, as described herein.

Any suitable hydrolyzed cellulosic material can be used in the fermentation step in practicing the present invention. The material is generally selected based on the desired fermentation product, i.e., the substance to be obtained from the fermentation, and the process employed, as is well known in the art.

The term “fermentation medium” is understood herein to refer to a medium before the fermenting microorganism(s) is(are) added, such as, a medium resulting from a saccharification process, as well as a medium used in a simultaneous saccharification and fermentation process (SSF).

“Fermenting microorganism” refers to any microorganism, including bacterial and fungal organisms, suitable for use in a desired fermentation process to produce a fermentation product. The fermenting organism can be hexose and/or pentose fermenting organisms, or a combination thereof. Both hexose and pentose fermenting organisms are well known in the art. Suitable fermenting microorganisms are able to ferment, i.e., convert, sugars, such as glucose, xylose, xylulose, arabinose, maltose, mannose, galactose, and/or oligosaccharides, directly or indirectly into the desired fermentation product. Examples of bacterial and fungal fermenting organisms producing ethanol are described by Lin et al., 2006, Appl. Microbiol. Biotechnol. 69: 627-642.

Examples of fermenting microorganisms that can ferment hexose sugars include bacterial and fungal organisms, such as yeast. Preferred yeast includes strains of Candida, Kluyveromyces, and Saccharomyces, e.g., Candida sonorensis, Kluyveromyces marxianus, and Saccharomyces cerevisiae.

Examples of fermenting organisms that can ferment pentose sugars in their native state include bacterial and fungal organisms, such as some yeast. Preferred xylose fermenting yeast include strains of Candida, preferably C. sheatae or C. sonorensis; and strains of Pichia, preferably P. stipitis, such as P. stipitis CBS 5773. Preferred pentose fermenting yeast include strains of Pachysolen, preferably P. tannophilus. Organisms not capable of fermenting pentose sugars, such as xylose and arabinose, may be genetically modified to do so by methods known in the art.

Examples of bacteria that can efficiently ferment hexose and pentose to ethanol include, for example, Bacillus coagulans, Clostridium acetobutylicum, Clostridium thermocellum, Clostridium phytofermentans, Geobacillus sp., Thermoanaerobacter saccharolyticum, and Zymomonas mobilis (Philippidis, 1996, supra).

Other fermenting organisms include strains of Bacillus, such as Bacillus coagulans; Candida, such as C. sonorensis, C. methanosorbosa, C. diddensiae, C. parapsilosis, C. naedodendra, C. blankii, C. entomophilia, C. brassicae, C. pseudotropicalis, C. boidinii, C. utifis, and C. scehatae; Clostridium, such as C. acetobutylicum, C. thermocellum, and C. phytofermentans; E. coli, especially E. coli strains that have been genetically modified to improve the yield of ethanol; Geobacillus sp.; Hansenula, such as Hansenula anomala; Klebsiella, such as K. oxytoca; Kluyveromyces, such as K. marxianus, K. lactis, K. thermotolerans, and K. fragilis; Schizosaccharomyces, such as S. pombe; Thermoanaerobacter, such as Thermoanaerobacter saccharolyticum; and Zymomonas, such as Zymomonas mobilis.

In a preferred aspect, the yeast is a Bretannomyces. In a more preferred aspect, the yeast is Bretannomyces clausenii. In another preferred aspect, the yeast is a Candida. In another more preferred aspect, the yeast is Candida sonorensis. In another more preferred aspect, the yeast is Candida boidinii. In another more preferred aspect, the yeast is Candida blankii. In another more preferred aspect, the yeast is Candida brassicae. In another more preferred aspect, the yeast is Candida diddensii. In another more preferred aspect, the yeast is Candida entomophiliia. In another more preferred aspect, the yeast is Candida pseudotropicalis. In another more preferred aspect, the yeast is Candida scehatae. In another more preferred aspect, the yeast is Candida utilis. In another preferred aspect, the yeast is a Clavispora. In another more preferred aspect, the yeast is Clavispora lusitaniae. In another more preferred aspect, the yeast is Clavispora opuntiae. In another preferred aspect, the yeast is a Kluyveromyces. In another more preferred aspect, the yeast is Kluyveromyces fragilis. In another more preferred aspect, the yeast is Kluyveromyces marxianus. In another more preferred aspect, the yeast is Kluyveromyces thermotolerans. In another preferred aspect, the yeast is a Pachysolen. In another more preferred aspect, the yeast is Pachysolen tannophilus. In another preferred aspect, the yeast is a Pichia. In another more preferred aspect, the yeast is a Pichia stipitis. In another preferred aspect, the yeast is a Saccharomyces spp. In another more preferred aspect, the yeast is Saccharomyces cerevisiae. In another more preferred aspect, the yeast is Saccharomyces distaticus. In another more preferred aspect, the yeast is Saccharomyces uvarum.

In a preferred aspect, the bacterium is a Bacillus. In a more preferred aspect, the bacterium is Bacillus coagulans. In another preferred aspect, the bacterium is a Clostridium. In another more preferred aspect, the bacterium is Clostridium acetobutylicum. In another more preferred aspect, the bacterium is Clostridium phytofermentans. In another more preferred aspect, the bacterium is Clostridium thermocellum. In another more preferred aspect, the bacterium is Geobacilus sp. In another more preferred aspect, the bacterium is a Thermoanaerobacter. In another more preferred aspect, the bacterium is Thermoanaerobacter saccharolyticum. In another preferred aspect, the bacterium is a Zymomonas. In another more preferred aspect, the bacterium is Zymomonas mobilis.

Commercially available yeast suitable for ethanol production include, e.g., BIOFERM™ AFT and XR (NABC—North American Bioproducts Corporation, GA, USA), ETHANOL RED™ yeast (Fermentis/Lesaffre, USA), FALI™ (Fleischmann's Yeast, USA), FERMIOL™ (DSM Specialties), GERT STRAND™ (Gert Strand AB, Sweden), and SUPERSTART™ and THERMOSACC™ fresh yeast (Ethanol Technology, WI, USA).

In a preferred aspect, the fermenting microorganism has been genetically modified to provide the ability to ferment pentose sugars, such as xylose utilizing, arabinose utilizing, and xylose and arabinose co-utilizing microorganisms.

The cloning of heterologous genes into various fermenting microorganisms has led to the construction of organisms capable of converting hexoses and pentoses to ethanol (co-fermentation) (Chen and Ho, 1993, Cloning and improving the expression of Pichia stipitis xylose reductase gene in Saccharomyces cerevisiae, Appl. Biochem. Biotechnol. 39-40: 135-147; Ho et al., 1998, Genetically engineered Saccharomyces yeast capable of effectively cofermenting glucose and xylose, Appl. Environ. Microbiol. 64: 1852-1859; Kotter and Ciriacy, 1993, Xylose fermentation by Saccharomyces cerevisiae, Appl. Microbiol. Biotechnol. 38: 776-783; Walfridsson et al., 1995, Xylose-metabolizing Saccharomyces cerevisiae strains overexpressing the TKL1 and TAL1 genes encoding the pentose phosphate pathway enzymes transketolase and transaldolase, Appl. Environ. Microbiol. 61: 4184-4190; Kuyper et al., 2004, Minimal metabolic engineering of Saccharomyces cerevisiae for efficient anaerobic xylose fermentation: a proof of principle, FEMS Yeast Research 4: 655-664; Beall et al., 1991, Parametric studies of ethanol production from xylose and other sugars by recombinant Escherichia coli, Biotech. Bioeng. 38: 296-303; Ingram et al., 1998, Metabolic engineering of bacteria for ethanol production, Biotechnol. Bioeng. 58: 204-214; Zhang et al., 1995, Metabolic engineering of a pentose metabolism pathway in ethanologenic Zymomonas mobilis, Science 267: 240-243; Deanda et al., 1996, Development of an arabinose-fermenting Zymomonas mobilis strain by metabolic pathway engineering, Appl. Environ. Microbiol. 62: 4465-4470; WO 2003/062430, xylose isomerase).

In a preferred aspect, the genetically modified fermenting microorganism is Candida sonorensis. In another preferred aspect, the genetically modified fermenting microorganism is Escherichia coli. In another preferred aspect, the genetically modified fermenting microorganism is Klebsiella oxytoca. In another preferred aspect, the genetically modified fermenting microorganism is Kluyveromyces marxianus. In another preferred aspect, the genetically modified fermenting microorganism is Saccharomyces cerevisiae. In another preferred aspect, the genetically modified fermenting microorganism is Zymomonas mobilis.

It is well known in the art that the organisms described above can also be used to produce other substances, as described herein.

The fermenting microorganism is typically added to the degraded cellulosic material or hydrolysate and the fermentation is performed for about 8 to about 96 hours, e.g., about 24 to about 60 hours. The temperature is typically between about 26° C. to about 60° C., e.g., about 32° C. or 50° C., and about pH 3 to about pH 8, e.g., pH 4-5, 6, or 7.

In one aspect, the yeast and/or another microorganism are applied to the degraded cellulosic material and the fermentation is performed for about 12 to about 96 hours, such as typically 24-60 hours. In another aspect, the temperature is preferably between about 20° C. to about 60° C., e.g., about 25° C. to about 50° C., about 32° C. to about 50° C., or about 32° C. to about 50° C., and the pH is generally from about pH 3 to about pH 7, e.g., about pH 4 to about pH 7. However, some fermenting organisms, e.g., bacteria, have higher fermentation temperature optima. Yeast or another microorganism is preferably applied in amounts of approximately 10⁵ to 10¹², preferably from approximately 10⁷ to 10¹⁰, especially approximately 2×10⁸ viable cell count per ml of fermentation broth. Further guidance in respect of using yeast for fermentation can be found in, e.g., “The Alcohol Textbook” (Editors K. Jacques, T. P. Lyons and D. R. Kelsall, Nottingham University Press, United Kingdom 1999), which is hereby incorporated by reference.

A fermentation stimulator can be used in combination with any of the processes described herein to further improve the fermentation process, and in particular, the performance of the fermenting microorganism, such as, rate enhancement and ethanol yield. A “fermentation stimulator” refers to stimulators for growth of the fermenting microorganisms, in particular, yeast. Preferred fermentation stimulators for growth include vitamins and minerals. Examples of vitamins include multivitamins, biotin, pantothenate, nicotinic acid, meso-inositol, thiamine, pyridoxine, para-aminobenzoic acid, folic acid, riboflavin, and Vitamins A, B, C, D, and E. See, for example, Alfenore et al., Improving ethanol production and viability of Saccharomyces cerevisiae by a vitamin feeding strategy during fed-batch process, Springer-Verlag (2002), which is hereby incorporated by reference. Examples of minerals include minerals and mineral salts that can supply nutrients comprising P, K, Mg, S, Ca, Fe, Zn, Mn, and Cu.

Fermentation Products:

A fermentation product can be any substance derived from the fermentation. The fermentation product can be, without limitation, an alcohol (e.g., arabinitol, n-butanol, isobutanol, ethanol, glycerol, methanol, ethylene glycol, 1,3-propanediol [propylene glycol], butanediol, glycerin, sorbitol, and xylitol); an alkane (e.g., pentane, hexane, heptane, octane, nonane, decane, undecane, and dodecane), a cycloalkane (e.g., cyclopentane, cyclohexane, cycloheptane, and cyclooctane), an alkene (e.g. pentene, hexene, heptene, and octene); an amino acid (e.g., aspartic acid, glutamic acid, glycine, lysine, serine, and threonine); a gas (e.g., methane, hydrogen (H₂), carbon dioxide (CO₂), and carbon monoxide (CO)); isoprene; a ketone (e.g., acetone); an organic acid (e.g., acetic acid, acetonic acid, adipic acid, ascorbic acid, citric acid, 2,5-diketo-D-gluconic acid, formic acid, fumaric acid, glucaric acid, gluconic acid, glucuronic acid, glutaric acid, 3-hydroxypropionic acid, itaconic acid, lactic acid, malic acid, malonic acid, oxalic acid, oxaloacetic acid, propionic acid, succinic acid, and xylonic acid); and polyketide. The fermentation product can also be protein as a high value product.

In a preferred aspect, the fermentation product is an alcohol. It will be understood that the term “alcohol” encompasses a substance that contains one or more hydroxyl moieties. In a more preferred aspect, the alcohol is n-butanol. In another more preferred aspect, the alcohol is isobutanol. In another more preferred aspect, the alcohol is ethanol. In another more preferred aspect, the alcohol is methanol. In another more preferred aspect, the alcohol is arabinitol. In another more preferred aspect, the alcohol is butanediol. In another more preferred aspect, the alcohol is ethylene glycol. In another more preferred aspect, the alcohol is glycerin. In another more preferred aspect, the alcohol is glycerol. In another more preferred aspect, the alcohol is 1,3-propanediol. In another more preferred aspect, the alcohol is sorbitol. In another more preferred aspect, the alcohol is xylitol. See, for example, Gong, C. S., Cao, N. J., Du, J., and Tsao, G. T., 1999, Ethanol production from renewable resources, in Advances in Biochemical Engineering/Biotechnology, Scheper, T., ed., Springer-Verlag Berlin Heidelberg, Germany, 65: 207-241; Silveira, M. M., and Jonas, R., 2002, The biotechnological production of sorbitol, Appl. Microbiol. Biotechnol. 59: 400-408; Nigam, P., and Singh, D., 1995, Processes for fermentative production of xylitol—a sugar substitute, Process Biochemistry 30 (2): 117-124; Ezeji, T. C., Qureshi, N. and Blaschek, H. P., 2003, Production of acetone, butanol and ethanol by Clostridium beijerinckii BA101 and in situ recovery by gas stripping, World Journal of Microbiology and Biotechnology 19 (6): 595-603.

In another preferred aspect, the fermentation product is an alkane. The alkane can be an unbranched or a branched alkane. In another more preferred aspect, the alkane is pentane. In another more preferred aspect, the alkane is hexane. In another more preferred aspect, the alkane is heptane. In another more preferred aspect, the alkane is octane. In another more preferred aspect, the alkane is nonane. In another more preferred aspect, the alkane is decane. In another more preferred aspect, the alkane is undecane. In another more preferred aspect, the alkane is dodecane.

In another preferred aspect, the fermentation product is a cycloalkane. In another more preferred aspect, the cycloalkane is cyclopentane. In another more preferred aspect, the cycloalkane is cyclohexane. In another more preferred aspect, the cycloalkane is cycloheptane. In another more preferred aspect, the cycloalkane is cyclooctane.

In another preferred aspect, the fermentation product is an alkene. The alkene can be an unbranched or a branched alkene. In another more preferred aspect, the alkene is pentene. In another more preferred aspect, the alkene is hexene. In another more preferred aspect, the alkene is heptene. In another more preferred aspect, the alkene is octene.

In another preferred aspect, the fermentation product is an amino acid. In another more preferred aspect, the organic acid is aspartic acid. In another more preferred aspect, the amino acid is glutamic acid. In another more preferred aspect, the amino acid is glycine. In another more preferred aspect, the amino acid is lysine. In another more preferred aspect, the amino acid is serine. In another more preferred aspect, the amino acid is threonine. See, for example, Richard, A., and Margaritis, A., 2004, Empirical modeling of batch fermentation kinetics for poly(glutamic acid) production and other microbial biopolymers, Biotechnology and Bioengineering 87 (4): 501-515.

In another preferred aspect, the fermentation product is a gas. In another more preferred aspect, the gas is methane. In another more preferred aspect, the gas is H₂. In another more preferred aspect, the gas is CO₂. In another more preferred aspect, the gas is CO. See, for example, Kataoka, N., A. Miya, and K. Kiriyama, 1997, Studies on hydrogen production by continuous culture system of hydrogen-producing anaerobic bacteria, Water Science and Technology 36 (6-7): 41-47; and Gunaseelan V. N. in Biomass and Bioenergy, Vol. 13 (1-2), pp. 83-114, 1997, Anaerobic digestion of biomass for methane production: A review.

In another preferred aspect, the fermentation product is isoprene.

In another preferred aspect, the fermentation product is a ketone. It will be understood that the term “ketone” encompasses a substance that contains one or more ketone moieties. In another more preferred aspect, the ketone is acetone. See, for example, Qureshi and Blaschek, 2003, supra.

In another preferred aspect, the fermentation product is an organic acid. In another more preferred aspect, the organic acid is acetic acid. In another more preferred aspect, the organic acid is acetonic acid. In another more preferred aspect, the organic acid is adipic acid. In another more preferred aspect, the organic acid is ascorbic acid. In another more preferred aspect, the organic acid is citric acid. In another more preferred aspect, the organic acid is 2,5-diketo-D-gluconic acid. In another more preferred aspect, the organic acid is formic acid. In another more preferred aspect, the organic acid is fumaric acid. In another more preferred aspect, the organic acid is glucaric acid. In another more preferred aspect, the organic acid is gluconic acid. In another more preferred aspect, the organic acid is glucuronic acid. In another more preferred aspect, the organic acid is glutaric acid. In another preferred aspect, the organic acid is 3-hydroxypropionic acid. In another more preferred aspect, the organic acid is itaconic acid. In another more preferred aspect, the organic acid is lactic acid. In another more preferred aspect, the organic acid is malic acid. In another more preferred aspect, the organic acid is malonic acid. In another more preferred aspect, the organic acid is oxalic acid. In another more preferred aspect, the organic acid is propionic acid. In another more preferred aspect, the organic acid is succinic acid. In another more preferred aspect, the organic acid is xylonic acid. See, for example, Chen, R., and Lee, Y. Y., 1997, Membrane-mediated extractive fermentation for lactic acid production from cellulosic biomass, Appl. Biochem. Biotechnol. 63-65: 435-448.

In another preferred aspect, the fermentation product is polyketide.

Recovery.

The fermentation product(s) can be optionally recovered from the fermentation medium using any method known in the art including, but not limited to, chromatography, electrophoretic procedures, differential solubility, distillation, or extraction. For example, alcohol is separated from the fermented cellulosic material and purified by conventional methods of distillation. Ethanol with a purity of up to about 96 vol. % can be obtained, which can be used as, for example, fuel ethanol, drinking ethanol, i.e., potable neutral spirits, or industrial ethanol.

Detergent Compositions

The present invention also relates to detergent compositions comprising a chimeric GH61 polypeptide of the present invention and a surfactant. The chimeric GH61 polypeptides having cellulolytic enhancing activity may be added to and thus become a component of a detergent composition.

The detergent composition of the present invention may be formulated, for example, as a hand or machine laundry detergent composition including a laundry additive composition suitable for pre-treatment of stained fabrics and a rinse added fabric softener composition, or be formulated as a detergent composition for use in general household hard surface cleaning operations, or be formulated for hand or machine dishwashing operations. In one aspect, the present invention also relates to methods for cleaning or washing a hard surface or laundry, the method comprising contacting the hard surface or the laundry with a detergent composition of the present invention.

In a specific aspect, the present invention provides a detergent additive comprising a chimeric GH61 polypeptide of the present invention. The detergent additive as well as the detergent composition may comprise one or more (e.g., several) enzymes selected from the group consisting of an amylase, arabinase, cutinase, carbohydrase, cellulase, galactanase, laccase, lipase, mannanase, oxidase, pectinase, peroxidase, protease, and xylanase.

In general the properties of the selected enzyme(s) should be compatible with the selected detergent, (i.e., pH-optimum, compatibility with other enzymatic and non-enzymatic ingredients, etc.), and the enzyme(s) should be present in effective amounts.

Cellulases:

Suitable cellulases include those of bacterial or fungal origin. Chemically modified or protein engineered mutants are included. Suitable cellulases include cellulases from the genera Bacillus, Pseudomonas, Humicola, Fusarium, Thielavia, Acremonium, e.g., the fungal cellulases produced from Humicola insolens, Myceliophthora thermophila and Fusarium oxysporum disclosed in U.S. Pat. No. 4,435,307, U.S. Pat. No. 5,648,263, U.S. Pat. No. 5,691,178, U.S. Pat. No. 5,776,757 and WO 89/09259.

Especially suitable cellulases are the alkaline or neutral cellulases having color care benefits. Examples of such cellulases are cellulases described in EP 0 495 257, EP 0 531 372, WO 96/11262, WO 96/29397, WO 98/08940. Other examples are cellulase variants such as those described in WO 94/07998, EP 0 531 315, U.S. Pat. No. 5,457,046, U.S. Pat. No. 5,686,593, U.S. Pat. No. 5,763,254, WO 95/24471, WO 98/12307 and PCT/DK98/00299.

Commercially available cellulases include CELLUZYME™, and CAREZYME™ (Novozymes A/S), CLAZINASE™, and PURADAX HA™ (Genencor International Inc.), and KAC-500(B)™ (Kao Corporation).

Proteases:

Suitable proteases include those of animal, vegetable or microbial origin. Microbial origin is preferred. Chemically modified or protein engineered mutants are included. The protease may be a serine protease or a metalloprotease, preferably an alkaline microbial protease or a trypsin-like protease. Examples of alkaline proteases are subtilisins, especially those derived from Bacillus, e.g., subtilisin Novo, subtilisin Carlsberg, subtilisin 309, subtilisin 147 and subtilisin 168 (described in WO 89/06279). Examples of trypsin-like proteases are trypsin (e.g., of porcine or bovine origin) and the Fusarium protease described in WO 89/06270 and WO 94/25583.

Examples of useful proteases are the variants described in WO 92/19729, WO 98/20115, WO 98/20116, and WO 98/34946, especially the variants with substitutions in one or more of the following positions: 27, 36, 57, 76, 87, 97, 101, 104, 120, 123, 167, 170, 194, 206, 218, 222, 224, 235, and 274.

Preferred commercially available protease enzymes include ALCALASE™, SAVINASE™, PRIMASET™, DURALASE™, ESPERASE™, and KANNASE™ (Novozymes A/S), MAXATASE™, MAXACAL™, MAXAPEM™, PROPERASE™, PURAFECT™, PURAFECT OXP™, FN2™, and FN3™ (Genencor International Inc.).

Lipases: Suitable lipases include those of bacterial or fungal origin. Chemically modified or protein engineered mutants are included. Examples of useful lipases include lipases from Humicola (synonym Thermomyces), e.g., from H. lanuginosa (T. lanuginosus) as described in EP 258 068 and EP 305 216 or from H. insolens as described in WO 96/13580, a Pseudomonas lipase, e.g., from P. alcaligenes or P. pseudoalcaligenes (EP 218 272), P. cepacia (EP 331 376), P. stutzeri (GB 1,372,034), P. fluorescens, Pseudomonas sp. strain SD 705 (WO 95/06720 and WO 96/27002), P. wisconsinensis (WO 96/12012), a Bacillus lipase, e.g., from B. subtilis (Dartois et al., 1993, Biochemica et Biophysica Acta, 1131: 253-360), B. stearothermophilus (JP 64/744992) or B. pumilus (WO 91/16422).

Other examples are lipase variants such as those described in WO 92/05249, WO 94/01541, EP 407 225, EP 260 105, WO 95/35381, WO 96/00292, WO 95/30744, WO 94/25578, WO 95/14783, WO 95/22615, WO 97/04079 and WO 97/07202.

Preferred commercially available lipase enzymes include LIPOLASE™ and LIPOLASE ULTRA™ (Novozymes A/S).

Amylases:

Suitable amylases (α and/or β) include those of bacterial or fungal origin. Chemically modified or protein engineered mutants are included. Amylases include, for example, α-amylases obtained from Bacillus, e.g., a special strain of Bacillus licheniformis, described in more detail in GB 1,296,839.

Examples of useful amylases are the variants described in WO 94/02597, WO 94/18314, WO 96/23873, and WO 97/43424, especially the variants with substitutions in one or more of the following positions: 15, 23, 105, 106, 124, 128, 133, 154, 156, 181, 188, 190, 197, 202, 208, 209, 243, 264, 304, 305, 391, 408, and 444.

Commercially available amylases are DURAMYL™, TERMAMYL™, FUNGAMYL™ and BAN™ (Novozymes A/S), RAPIDASE™ and PURASTAR™ (from Genencor International Inc.).

Peroxidases/Oxidases:

Suitable peroxidases/oxidases include those of plant, bacterial or fungal origin. Chemically modified or protein engineered mutants are included. Examples of useful peroxidases include peroxidases from Coprinus, e.g., from C. cinereus, and variants thereof as those described in WO 93/24618, WO 95/10602, and WO 98/15257.

Commercially available peroxidases include GUARDZYME™ (Novozymes A/S).

The detergent enzyme(s) may be included in a detergent composition by adding separate additives containing one or more (e.g., several) enzymes, or by adding a combined additive comprising all of these enzymes. A detergent additive of the invention, i.e., a separate additive or a combined additive, can be formulated, for example, as a granulate, liquid, slurry, etc. Preferred detergent additive formulations are granulates, in particular non-dusting granulates, liquids, in particular stabilized liquids, or slurries.

Non-dusting granulates may be produced, e.g., as disclosed in U.S. Pat. Nos. 4,106,991 and 4,661,452 and may optionally be coated by methods known in the art. Examples of waxy coating materials are poly(ethylene oxide) products (polyethyleneglycol, PEG) with mean molar weights of 1000 to 20000; ethoxylated nonylphenols having from 16 to 50 ethylene oxide units; ethoxylated fatty alcohols in which the alcohol contains from 12 to 20 carbon atoms and in which there are 15 to 80 ethylene oxide units; fatty alcohols; fatty acids; and mono- and di- and triglycerides of fatty acids. Examples of film-forming coating materials suitable for application by fluid bed techniques are given in GB 1483591. Liquid enzyme preparations may, for instance, be stabilized by adding a polyol such as propylene glycol, a sugar or sugar alcohol, lactic acid or boric acid according to established methods. Protected enzymes may be prepared according to the method disclosed in EP 238,216.

The detergent composition of the invention may be in any convenient form, e.g., a bar, a tablet, a powder, a granule, a paste, or a liquid. A liquid detergent may be aqueous, typically containing up to 70% water and 0-30% organic solvent, or non-aqueous.

The detergent composition comprises one or more (e.g., several) surfactants, which may be non-ionic including semi-polar and/or anionic and/or cationic and/or zwitterionic. The surfactants are typically present at a level of from 0.1% to 60% by weight.

When included therein the detergent will usually contain from about 1% to about 40% of an anionic surfactant such as linear alkylbenzenesulfonate, alpha-olefinsulfonate, alkyl sulfate (fatty alcohol sulfate), alcohol ethoxysulfate, secondary alkanesulfonate, alpha-sulfo fatty acid methyl ester, alkyl- or alkenylsuccinic acid, or soap.

When included therein the detergent will usually contain from about 0.2% to about 40% of a non-ionic surfactant such as alcohol ethoxylate, nonylphenol ethoxylate, alkylpolyglycoside, alkyldimethylamineoxide, ethoxylated fatty acid monoethanolamide, fatty acid monoethanolamide, polyhydroxy alkyl fatty acid amide, or N-acyl N-alkyl derivatives of glucosamine (“glucamides”).

The detergent may contain 0-65% of a detergent builder or complexing agent such as zeolite, diphosphate, triphosphate, phosphonate, carbonate, citrate, nitrilotriacetic acid, ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, alkyl- or alkenylsuccinic acid, soluble silicates, or layered silicates (e.g., SKS-6 from Hoechst).

The detergent may comprise one or more (e.g., several) polymers. Examples are carboxymethylcellulose, poly(vinylpyrrolidone), poly (ethylene glycol), poly(vinyl alcohol), poly(vinylpyridine-N-oxide), poly(vinylimidazole), polycarboxylates such as polyacrylates, maleic/acrylic acid copolymers, and lauryl methacrylate/acrylic acid copolymers.

The detergent may contain a bleaching system which may comprise a H₂O₂ source such as perborate or percarbonate which may be combined with a peracid-forming bleach activator such as tetraacetylethylenediamine or nonanoyloxybenzenesulfonate. Alternatively, the bleaching system may comprise peroxyacids of, for example, the amide, imide, or sulfone type.

The enzyme(s) of the detergent composition of the invention may be stabilized using conventional stabilizing agents, e.g., a polyol such as propylene glycol or glycerol, a sugar or sugar alcohol, lactic acid, boric acid, or a boric acid derivative, e.g., an aromatic borate ester, or a phenyl boronic acid derivative such as 4-formylphenyl boronic acid, and the composition may be formulated as described in, for example, WO 92/19709 and WO 92/19708.

The detergent may also contain other conventional detergent ingredients such as, e.g., fabric conditioners including clays, foam boosters, suds suppressors, anti-corrosion agents, soil-suspending agents, anti-soil redeposition agents, dyes, bactericides, optical brighteners, hydrotropes, tarnish inhibitors, or perfumes.

In the detergent compositions, any enzyme may be added in an amount corresponding to 0.01-100 mg of enzyme protein per liter of wash liquor, preferably 0.05-5 mg of enzyme protein per liter of wash liquor, in particular 0.1-1 mg of enzyme protein per liter of wash liquor.

In the detergent compositions, a chimeric GH61 polypeptide of the present invention having cellulolytic enhancing activity may be added in an amount corresponding to 0.001-100 mg of protein, preferably 0.005-50 mg of protein, more preferably 0.01-25 mg of protein, even more preferably 0.05-10 mg of protein, most preferably 0.05-5 mg of protein, and even most preferably 0.01-1 mg of protein per liter of wash liquor.

A chimeric GH61 polypeptide of the present invention having cellulolytic enhancing activity may also be incorporated in the detergent formulations disclosed in WO 97/07202, which is hereby incorporated by reference.

Plants

The present invention also relates to plants, e.g., a transgenic plant, plant part, or plant cell, comprising a polynucleotide of the present invention so as to express and produce the chimeric GH61 polypeptide in recoverable quantities. The chimeric GH61 polypeptide may be recovered from the plant or plant part. Alternatively, the plant or plant part containing the chimeric GH61 polypeptide may be used as such for improving the quality of a food or feed, e.g., improving nutritional value, palatability, and rheological properties, or to destroy an antinutritive factor.

The present invention also relates to isolated plants, e.g., a transgenic plant, plant part, or plant cell, comprising a polynucleotide of the present invention so as to express and produce a chimeric GH61 polypeptide in recoverable quantities. The chimeric GH61 polypeptide may be recovered from the plant or plant part. Alternatively, the plant or plant part containing the chimeric GH61 polypeptide may be used as such for improving the quality of a food or feed, e.g., improving nutritional value, palatability, and rheological properties, or to destroy an antinutritive factor.

The transgenic plant can be dicotyledonous (a dicot) or monocotyledonous (a monocot). Examples of monocot plants are grasses, such as meadow grass (blue grass, Poa), forage grass such as Festuca, Lolium, temperate grass, such as Agrostis, and cereals, e.g., wheat, oats, rye, barley, rice, sorghum, and maize (corn).

Examples of dicot plants are tobacco, legumes, such as lupins, potato, sugar beet, pea, bean and soybean, and cruciferous plants (family Brassicaceae), such as cauliflower, rape seed, and the closely related model organism Arabidopsis thaliana.

Examples of plant parts are stem, callus, leaves, root, fruits, seeds, and tubers as well as the individual tissues comprising these parts, e.g., epidermis, mesophyll, parenchyme, vascular tissues, meristems. Specific plant cell compartments, such as chloroplasts, apoplasts, mitochondria, vacuoles, peroxisomes and cytoplasm are also considered to be a plant part. Furthermore, any plant cell, whatever the tissue origin, is considered to be a plant part. Likewise, plant parts such as specific tissues and cells isolated to facilitate the utilization of the invention are also considered plant parts, e.g., embryos, endosperms, aleurone and seed coats.

Also included within the scope of the present invention are the progeny of such plants, plant parts, and plant cells.

The transgenic plant or plant cell expressing the chimeric GH61 polypeptide may be constructed in accordance with methods known in the art. In short, the plant or plant cell is constructed by incorporating one or more expression constructs encoding the chimeric GH61 polypeptide into the plant host genome or chloroplast genome and propagating the resulting modified plant or plant cell into a transgenic plant or plant cell.

The expression construct is conveniently a nucleic acid construct that comprises a polynucleotide encoding a chimeric GH61 polypeptide operably linked with appropriate regulatory sequences required for expression of the polynucleotide in the plant or plant part of choice. Furthermore, the expression construct may comprise a selectable marker useful for identifying plant cells into which the expression construct has been integrated and DNA sequences necessary for introduction of the construct into the plant in question (the latter depends on the DNA introduction method to be used).

The choice of regulatory sequences, such as promoter and terminator sequences and optionally signal or transit sequences, is determined, for example, on the basis of when, where, and how the chimeric GH61 polypeptide is desired to be expressed. For instance, the expression of the gene encoding a polypeptide may be constitutive or inducible, or may be developmental, stage or tissue specific, and the gene product may be targeted to a specific tissue or plant part such as seeds or leaves. Regulatory sequences are, for example, described by Tague et al., 1988, Plant Physiology 86: 506.

For constitutive expression, the 35S-CaMV, the maize ubiquitin 1, or the rice actin 1 promoter may be used (Franck et al., 1980, Cell 21: 285-294; Christensen et al., 1992, Plant Mol. Biol. 18: 675-689; Zhang et al., 1991, Plant Cell 3: 1155-1165). Organ-specific promoters may be, for example, a promoter from storage sink tissues such as seeds, potato tubers, and fruits (Edwards and Coruzzi, 1990, Ann. Rev. Genet. 24: 275-303), or from metabolic sink tissues such as meristems (Ito et al., 1994, Plant Mol. Biol. 24: 863-878), a seed specific promoter such as the glutelin, prolamin, globulin, or albumin promoter from rice (Wu et al., 1998, Plant Cell Physiol. 39: 885-889), a Vicia faba promoter from the legumin B4 and the unknown seed protein gene from Vicia faba (Conrad et al., 1998, J. Plant Physiol. 152: 708-711), a promoter from a seed oil body protein (Chen et al., 1998, Plant Cell Physiol. 39: 935-941), the storage protein napA promoter from Brassica napus, or any other seed specific promoter known in the art, e.g., as described in WO 91/14772. Furthermore, the promoter may be a leaf specific promoter such as the rbcs promoter from rice or tomato (Kyozuka et al., 1993, Plant Physiol. 102: 991-1000), the chlorella virus adenine methyltransferase gene promoter (Mitra and Higgins, 1994, Plant Mol. Biol. 26: 85-93), the aldP gene promoter from rice (Kagaya et al., 1995, Mol. Gen. Genet. 248: 668-674), or a wound inducible promoter such as the potato pin2 promoter (Xu et al., 1993, Plant Mol. Biol. 22: 573-588). Likewise, the promoter may be induced by abiotic treatments such as temperature, drought, or alterations in salinity or induced by exogenously applied substances that activate the promoter, e.g., ethanol, oestrogens, plant hormones such as ethylene, abscisic acid, and gibberellic acid, and heavy metals.

A promoter enhancer element may also be used to achieve higher expression of a chimeric GH61 polypeptide in the plant. For instance, the promoter enhancer element may be an intron that is placed between the promoter and the polynucleotide encoding a chimeric GH61 polypeptide. For instance, Xu et al., 1993, supra, disclose the use of the first intron of the rice actin 1 gene to enhance expression.

The selectable marker gene and any other parts of the expression construct may be chosen from those available in the art.

The nucleic acid construct is incorporated into the plant genome according to conventional techniques known in the art, including Agrobacterium-mediated transformation, virus-mediated transformation, microinjection, particle bombardment, biolistic transformation, and electroporation (Gasser et al., 1990, Science 244: 1293; Potrykus, 1990, Bio/Technology 8: 535; Shimamoto et al., 1989, Nature 338: 274).

Agrobacterium tumefaciens-mediated gene transfer is a method for generating transgenic dicots (for a review, see Hooykas and Schilperoort, 1992, Plant Mol. Biol. 19: 15-38) and for transforming monocots, although other transformation methods may be used for these plants. A method for generating transgenic monocots is particle bombardment (microscopic gold or tungsten particles coated with the transforming DNA) of embryonic calli or developing embryos (Christou, 1992, Plant J. 2: 275-281; Shimamoto, 1994, Curr. Opin. Biotechnol. 5: 158-162; Vasil et al., 1992, Bio/Technology 10: 667-674). An alternative method for transformation of monocots is based on protoplast transformation as described by Omirulleh et al., 1993, Plant Mol. Biol. 21: 415-428. Additional transformation methods include those described in U.S. Pat. Nos. 6,395,966 and 7,151,204 (both of which are herein incorporated by reference in their entirety).

Following transformation, the transformants having incorporated the expression construct are selected and regenerated into whole plants according to methods well known in the art. Often the transformation procedure is designed for the selective elimination of selection genes either during regeneration or in the following generations by using, for example, co-transformation with two separate T-DNA constructs or site specific excision of the selection gene by a specific recombinase.

In addition to direct transformation of a particular plant genotype with a construct of the present invention, transgenic plants may be made by crossing a plant having the construct to a second plant lacking the construct. For example, a construct encoding a chimeric GH61 polypeptide can be introduced into a particular plant variety by crossing, without the need for ever directly transforming a plant of that given variety. Therefore, the present invention encompasses not only a plant directly regenerated from cells which have been transformed in accordance with the present invention, but also the progeny of such plants. As used herein, progeny may refer to the offspring of any generation of a parent plant prepared in accordance with the present invention. Such progeny may include a DNA construct prepared in accordance with the present invention. Crossing results in the introduction of a transgene into a plant line by cross pollinating a starting line with a donor plant line. Non-limiting examples of such steps are described in U.S. Pat. No. 7,151,204.

Plants may be generated through a process of backcross conversion. For example, plants include plants referred to as a backcross converted genotype, line, inbred, or hybrid.

Genetic markers may be used to assist in the introgression of one or more transgenes of the invention from one genetic background into another. Marker assisted selection offers advantages relative to conventional breeding in that it can be used to avoid errors caused by phenotypic variations. Further, genetic markers may provide data regarding the relative degree of elite germplasm in the individual progeny of a particular cross. For example, when a plant with a desired trait which otherwise has a non-agronomically desirable genetic background is crossed to an elite parent, genetic markers may be used to select progeny which not only possess the trait of interest, but also have a relatively large proportion of the desired germplasm. In this way, the number of generations required to introgress one or more traits into a particular genetic background is minimized.

The present invention also relates to methods of producing a chimeric GH61 polypeptide of the present invention comprising (a) cultivating a transgenic plant or a plant cell comprising a polynucleotide encoding the chimeric GH61 polypeptide under conditions conducive for production of the chimeric GH61 polypeptide; and (b) recovering the chimeric GH61 polypeptide.

The present invention is further described by the following examples that should not be construed as limiting the scope of the invention.

EXAMPLES Media and Solutions

PDA plates were composed of 39 g of potato dextrose agar and deionized water to 1 liter.

MDU2BP medium was composed of 45 g of maltose, 1 g of MgSO₄.7H₂O, 1 g of NaCl, 2 g of K₂HSO₄, 12 g of KH₂PO₄, 2 g of urea, 500 μl of AMG trace metals solution, and deionized water to 1 liter (pH 5.0).

AMG trace metals solution was composed of 14.3 g of ZnSO₄.7H₂O, 2.5 g of CuSO₄.5H₂O, 0.5 g of NiCl₂.6H₂O, 13.8 g of FeSO₄.H₂O, 8.5 g of MnSO₄.7H₂O, 3 g of citric acid, and deionized water to 1 liter.

M410 medium was composed of 50 g of maltose, 50 g of glucose, 2 g of MgSO₄.7H₂O, 2 g of KH₂PO₄, 4 g of citric acid anhydrous powder, 8 g of yeast extract, 2 g of urea, 0.5 g of AMG trace metals solution, 0.5 g of CaCl₂, and deionized water to 1 liter (pH 6.0).

YPG medium was composed of 10 g of yeast extract, 10 g of Bacto peptone, 20 g of glucose, and deionized water to 1 liter.

YPM medium was composed of 1% yeast extract, 2% of peptone, and 2% of maltose in deionized water.

LB plates were composed of 10 g of Bacto-tryptone. 5 g of yeast extract, 10 g of sodium chloride, 15 g of Bacto-agar, and deionized water to 1 liter.

COVE plates were composed of 342.3 g of sucrose, 25 g of Noble agar, 20 ml of COVE salts solution, 10 mM acetamide, 15 or 20 mM CsCl, and deionized water to 1 liter. The solution was adjusted to pH 7.0 before autoclaving.

COVE2 plates were composed of 30 g of sucrose, 20 ml of COVE salts solution, 20 ml of 1 M acetamide, 25 g of Agar Noble, and deionized water to 1 liter.

COVE salts solution was composed of 26 g of KCl, 26 g of MgSO₄.7H₂O, 76 g of KH₂PO₄, 0 ml of COVE trace metals solution, and deionized water to 1 liter.

COVE trace metals solution was composed of 0.04 g of Na₂B₄O₇.10H₂O, 0.4 g of CuSO₄.5H₂O, 1.2 g of FeSO₄.7H₂O, 0.7 g of MnSO₄.H₂O, 0.8 g of Na₂MoO₂.2H₂O, 10 g of ZnSO₄.7H₂O, and deionized water to 1 liter.

Cellulase-inducing medium was composed of 20 g of cellulose, 10 g of corn steep solids, 1.45 g of (NH₄)₂SO₄, 2.08 g of KH₂PO₄, 0.28 g of CaCl₂, 0.42 g of MgSO₄.7H₂O, 0.42 ml of Trichoderma trace metals solution, 1-2 drops of antifoam, and deionized water to 1 liter.

Trichoderma trace metals solution was composed of 216 g of FeCl₃.6H₂O, 58 g of ZnSO₄.7H₂O, 27 g of MnSO₄.H₂O, 10 g of CuSO₄.5H₂O, 2.4 g of H₃BO₃, 336 g of citric acid, and deionized water to 1 liter.

PEG buffer was composed of 500 g of polyethylene glycol 4000 (PEG 4000), 10 mM CaCl₂, 10 mM Tris-HCl pH 7.5, and deionized water to 1 liter; filter sterilized.

STC was composed of 1 M sorbitol, 10 mM CaCl₂, and 10 mM Tris-HCl, pH 7.5 in deionized water; filter sterilized.

Example 1 Preparation of Aspergillus fumigatus GH61B Polypeptide Having Cellulolytic Enhancing Activity

The Aspergillus fumigatus polypeptide having cellulolytic enhancing activity (SEQ ID NO: 93 [DNA sequence] and SEQ ID NO: 94 [deduced amino acid sequence]) was prepared as described below.

A tblastn search (Altschul et al., 1997, Nucleic Acids Res. 25: 3389-3402) of the A. fumigatus partial genome sequence (The Institute for Genomic Research, Rockville, Md., USA) was performed using as query several known GH61 polypeptides including the Thermoascus aurantiacus GH61A polypeptide (GeneSeqP Accession Number AEC05922). Several genes were identified as putative Family GH61 homologs based upon a high degree of similarity to the query sequences at the amino acid level. One genomic region of approximately 850 bp with greater than 70% sequence identity to the Thermoascus aurantiacus GH61A polypeptide amino acid sequence was chosen for further study.

A. fumigatus NN051616 was grown and harvested as described in U.S. Pat. No. 7,244,605. Frozen mycelia were ground, by mortar and pestle, to a fine powder and genomic DNA was isolated using a DNEASY® Plant Maxi Kit (QIAGEN Inc., Valencia, Calif., USA) according to manufacturer's instructions.

Two synthetic oligonucleotide primers shown below were designed to PCR amplify the A. fumigatus Family GH61B polypeptide gene from the genomic DNA. An IN-FUSION® Cloning Kit (BD Biosciences, Palo Alto, Calif., USA) was used to clone the fragment directly into the expression vector pAILo2 (WO 2004/099228), without the need for restriction digestion and ligation.

Forward primer: (SEQ ID NO: 133) 5′-ACTGGATTTACCATGACTTTGTCCAAGATCACTTCCA-3′ Reverse primer: (SEQ ID NO: 134) 5′-TCACCTCTAGTTAATTAAGCGTTGAACAGTGCAGGACCAG-3′ Bold letters represent coding sequence. The remaining sequence is homologous to the insertion sites of pAILo2.

Fifty picomoles of each of the primers above were used in a PCR reaction composed of 204 ng of A. fumigatus genomic DNA, 1×Pfx Amplification Buffer (Invitrogen, Carlsbad, Calif., USA), 1.5 μl of a 10 mM blend of dATP, dTTP, dGTP, and dCTP, 2.5 units of PLATINUM® Pfx DNA polymerase (Invitrogen Corp., Carlsbad, Calif., USA), and 1 μl of 50 mM MgSO₄ in a final volume of 50 μl. The amplification was performed using an EPPENDORF® MASTERCYCLER® 5333 epgradient S (Eppendorf Scientific, Inc., Westbury, N.Y., USA) programmed for 1 cycle at 94° C. for 3 minutes; and 30 cycles each at 94° C. for 30 seconds, 56° C. for 30 seconds, and 72° C. for 1 minutes. The heat block was then held at 72° C. for 15 minutes followed by a 4° C. soak cycle.

The reaction products were isolated by 1.0% agarose gel electrophoresis using 40 mM Tris base-20 mM sodium acetate-1 mM disodium EDTA (TAE) buffer where an approximately 850 bp product band was excised from the gel and purified using a MINELUTE® Gel Extraction Kit (QIAGEN Inc., Valencia, Calif., USA) according to the manufacturer's instructions.

The fragment was then cloned into pAILo2 using an IN-FUSION® Cloning Kit. The vector was digested with Nco I and Pac I and the fragment was purified by gel electrophoresis as above and a QIAQUICK® Gel Purification Kit (QIAGEN Inc., Valencia, Calif., USA). The gene fragment and the digested vector were combined together in a reaction resulting in the expression plasmid pAG43 in which transcription of the Family GH61B polypeptide gene was under the control of the NA2-tpi promoter. The NA2-tpi promoter is a modified promoter from the Aspergillus niger neutral alpha-amylase gene in which the untranslated leader has been replaced by an untranslated leader from the Aspergillus nidulans triose phosphate isomerase gene. The recombination reaction (20 μl) was composed of 1×IN-FUSION® Buffer (BD Biosciences, Palo Alto, Calif., USA), 1×BSA (BD Biosciences, Palo Alto, Calif., USA), 1 μl of IN-FUSION® enzyme (diluted 1:10) (BD Biosciences, Palo Alto, Calif., USA), 166 ng of pAILo2 digested with Nco I and Pac I, and 110 ng of the A. fumigatus GH61B polypeptide purified PCR product. The reaction was incubated at 37° C. for 15 minutes followed by 15 minutes at 50° C. The reaction was diluted with 40 μl of 10 mM Tris-0.1 M EDTA buffer and 2.5 μl of the diluted reaction was used to transform E. coli XL10 SOLOPACK® Gold competent cells (Stratagene, La Jolla, Calif., USA). An E. coli transformant containing pAG43 (GH61B protein gene) was identified by restriction enzyme digestion and plasmid DNA was prepared using a BIOROBOT® 9600 (QIAGEN Inc., Valencia, Calif., USA).

DNA sequencing of the 862 bp PCR fragment was performed with an Applied Biosystems Model 377 XL Automated DNA Sequencer (Applied Biosystems, Carlsbad, Calif., USA) using dye-terminator chemistry (Giesecke et al., 1992, Journal of Virology Methods 38: 47-60) and primer walking strategy. The following vector specific primers were used for sequencing:

pAllo2 5 Seq: (SEQ ID NO: 135) 5′-TGTCCCTTGTCGATGCG 3′ pAllo2 3 Seq: (SEQ ID NO: 136) 5′-CACATGACTTGGCTTCC 3′

Nucleotide sequence data were scrutinized for quality and all sequences were compared to each other with assistance of PHRED/PHRAP software (University of Wash., Seattle, Wash., USA).

A gene model for the A. fumigatus sequence was constructed based on similarity of the encoded protein to the Thermoascus aurantiacus GH61A polypeptide (GeneSeqP Accession Number AEC05922). The nucleotide sequence and deduced amino acid sequence of the A. fumigatus GH61B polypeptide gene are shown in SEQ ID NO: 93 and SEQ ID NO: 94, respectively. The genomic fragment encodes a polypeptide of 250 amino acids, interrupted by 2 introns of 53 and 56 bp. The % G+C content of the gene and the mature coding sequence are 53.9% and 57%, respectively. Using the SignalP software program (Nielsen et al., 1997, Protein Engineering 10:1-6), a signal peptide of 21 residues was predicted. The predicted mature protein contains 229 amino acids with a predicted molecular mass of 23.39 kDa.

Aspergillus oryzae JaL355 protoplasts prepared according to the method of Christensen et al., 1988, Bio/Technology 6: 1419-1422, were transformed with 6 μg of pAG43. Twenty-six transformants were isolated to individual PDA plates.

Confluent PDA plates of 24 of the transformants were each washed with 5 ml of 0.01% TWEEN® 20 and the spores were each collected. Eight μl of each spore stock was added to 1 ml of YPG, YPM, and M410 media separately in 24 well plates and incubated at 34° C. After 3 days of incubation, 7.5 μl of supernatant from four transformants were analyzed using a CRITERION® stain-free, 8-16% gradient SDS-PAGE gel (Bio-Rad Laboratories, Inc., Hercules, Calif., USA) according to the manufacturer's instructions. Based on this gel, M410 medium was chosen as the best medium. Five days after incubation, 7.5 μl of supernatant from each M410 culture was analyzed using a CRITERION® stain-free, 8-16% gradient SDS-PAGE gel. SDS-PAGE profiles of the cultures showed that several transformants had a new major band at approximately 25 kDa.

A confluent plate of one transformant (grown on a PDA plate) was washed with 5 ml of 0.01% TWEEN® 20 and inoculated into four 500 ml Erlenmeyer flasks containing 100 ml of M410 medium to generate broth for characterization of the enzyme. The flasks were harvested on day 5 (300 ml), filtered using a 0.22 μm EXPRESS™ Plus Membrane (Millipore, Bedford, Mass., USA), and stored at 4° C.

The filtered shake flask broth containing the recombinantly produced A. fumigatus GH61B polypeptide having cellulolytic enhancing activity was first concentrated by a tangential flow concentrator (Pall Filtron, Northborough, Mass., USA) equipped with a 10 kDa polyethersulfone membrane (Pall Filtron, Northborough, Mass., USA), buffer exchanged into 20 mM Tris-HCl pH 8.0, and then purified using a HILOAD™ 26/60 SUPERDEX™ 75 gel filtration column (GE Healthcare, Piscataway, N.J., USA) with a 750 ml isocratic gradient in 150 mM NaCl, 20 mM Tris-HCl pH 8.0. Fractions were collected and pooled based on SDS-PAGE. Protein concentration was determined using a Microplate BCA™ Protein Assay Kit (Thermo Fisher Scientific Inc., Rockford, Ill., USA) in which bovine serum albumin was used as a protein standard.

Example 2 Construction of an Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A Chimeric Polypeptide Having Cellulolytic Enhancing Activity

An Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A chimeric polypeptide having cellulolytic enhancing activity was constructed and expressed in Aspergillus oryzae JaL250. The chimeric GH61 polypeptide combines three different fragments of the A. fumigatus GH61B polypeptide and the T. aurantiacus GH61A polypeptide. The first GH61 fragment contains amino acids 1 to 84 of SEQ ID NO: 78 of the T. aurantiacus GH61A polypeptide (amino acids 1 to 21 are the signal peptide), the second GH61 fragment contains amino acids 85 to 207 of SEQ ID NO: 94 of the A. fumigatus GH61B polypeptide, and the third GH61 fragment contains amino acids 208 to 249 of SEQ ID NO: 78 of the T. aurantiacus GH61A polypeptide. The polynucleotides encoding the first and third fragments were PCR amplified from plasmid pDZA2 (WO 2005/074656), an A. oryzae expression vector comprising the polynucleotide encoding wild-type T. aurantiacus GH61A polypeptide, and the polynucleotide encoding the second fragment was PCR amplified from plasmid pAG43, an A. oryzae expression vector containing the polynucleotide encoding wild-type Aspergillus fumigatus GH61B polypeptide described in Example 1. Plasmid pCW026 (WO 2005/030926) is an Aspergillus oryzae expression vector comprising the polynucleotide encoding wild-type Trichoderma reesei CEL7A cellobiohydrolase. The PCR amplified sections for the first, second, and third GH61 polypeptide fragments were then subcloned simultaneously into plasmid pCW026 (gapped with Pac I and Pst I) according to the method of Zhu et al., 2007, BioTechniques 43: 354-359 and an IN-FUSION™ Advantage PCR Cloning Kit (Clontech Laboratories, Inc., Mountain View, Calif., USA) with the primers shown below. The primers were designed to amplify the polynucleotide for the first GH61 polypeptide fragment from the 5′ end of the polynucleotide in plasmid pDZA2 encoding the T. aurantiacus GH61A polypeptide.

Forward primer (5AF): (SEQ ID NO: 137) 5′-AACCACAAATCACAGTCGTCCCCGGTATTG-3′ Reverse primer (5AR): (SEQ ID NO: 138) 5′-GGTTGCGGTCAACTTTCCAGGCTTGGCGCCCCTATGGCA-3′

Primer 5AF was designed to prime more than 30 bp upstream of the unique Pst I restriction enzyme site on plasmid pDZA2 and primer 5AR was designed to contain a 24 bp region corresponding to amino acids 77-84 of the T. aurantiacus GH61A polypeptide in addition to a 15 bp region corresponding to amino acids 85-89 of the A. fumigatus GH61B polypeptide.

The primers shown below were designed to amplify the polynucleotide for the second GH61 polypeptide fragment from the polynucleotide in plasmid pAG43 encoding the A. fumigatus GH61B polypeptide.

Forward primer (5BF): (SEQ ID NO: 139) 5′-GGCGCCAAGCCTGGAAAGTTGACCGCAACCGTTGCAGCC-3′ Reverse primer (5BR): (SEQ ID NO: 140) 5′-AGGGTTATCAGAACCGCCACCGGTGATTTGGATGTTGAA-3′

Primer 5BF was designed to contain a 15 bp region encoding amino acids 79-84 of the T. aurantiacus GH61A polypeptide in addition to a 24 bp region encoding amino acids 85-92 of the A. fumigatus GH61B polypeptide. Primer 5BF was designed to contain a 24 bp region encoding amino acids 200-207 of the A. fumigatus GH61B polypeptide in addition to a 15 bp region encoding amino acids 208-212 of the T. aurantiacus GH61A polypeptide.

The primers shown below were designed to amplify the polynucleotide for the third GH61 polypeptide fragment from the polynucleotide in plasmid pDZA2 encoding the T. aurantiacus GH61A polypeptide.

Forward primer (5CF): (SEQ ID NO: 141) 5′-CAAATCACCGGTGGCGGTTCTGATAACCCTGCTGGAACT-3′ Reverse primer (5CR): (SEQ ID NO: 142) 5′-CAGGTGTCAGTCACCTCTAGTTAATTAATTAACCAGTATACAGAGGA GGACCAGGGATGAT-3′

Primer 5CF was designed to contain a 15 bp region encoding amino acids 203-207 of the A. fumigatus GH61B polypeptide in addition to a 24 bp region corresponding to amino acids 208-215 of the T. aurantiacus GH61A polypeptide. Primer 5CR was designed to contain a 33 bp region corresponding to amino acids 239-249 of the T. aurantiacus GH61A polypeptide in addition to a 23 bp region which includes the Pac I restriction enzyme site and the 5′ end of the AMG terminator from plasmid pCW026.

Chimeric DNA Predicted PCR section Oligo pairs template size (bp) First fragment 068393 + 068400 pDZA2 555 Second fragment 068401 + 068406 pAG43 455 Third fragment 068407 + 068399 pDZA2 181

A total of 50 picomoles of each of the primers above were used in an amplification reaction composed of 50 ng of pDZA2 or pAG43, 1× AMPLITAQ GOLD® Buffer II (Applied Biosystems, Foster City, Calif., USA), 1 μl of a blend of dATP, dTTP, dGTP, and dCTP, each at 10 mM, 5 units of AMPLITAQ GOLD® DNA polymerase (Applied Biosystems, Foster City, Calif., USA), and 3 μl of 25 mM MgSO₄ in a final volume of 50 μl. The amplification reaction was performed in an EPPENDORF® MASTERCYCLER® 5333 (Eppendorf EG, Hamburg, Germany) programmed for 1 cycle at 95° C. for 9 minutes; and 30 cycles each at 95° C. for 30 seconds, 55° C. for 30 seconds, and 72° C. for 30 seconds. After the 30 cycles, the reaction was heated for 5 minutes at 72° C. The heat block then went to a 10° C. soak cycle.

The reaction products were isolated by 1.0% agarose gel electrophoresis using TAE buffer where a 555 bp PCR product band for the first GH61 polypeptide fragment, a 455 bp PCR product band for the second GH61 polypeptide fragment, and a 181 bp PCR product band for the third GH61 polypeptide fragment were excised from the gel and extracted using a QIAQUICK® Gel Extraction Kit (QIAGEN Inc., Valencia, Calif., USA).

Plasmid pCW026 was gapped by digestion with Pac I and Pst I. The digestion was verified by fractionating an aliquot of the digestion by 0.8% agarose gel electrophoresis in TAE buffer where expected fragments of 5569 bp (gapped) and 1751 bp (3′ end of the TAKA promoter and Trichoderma reesei CEL7A cellobiohydrolase gene) were obtained. The 5569 bp (gapped) fragment was excised from the gel and purified using a QIAQUICK® Gel Extraction Kit.

Multi-fragment PCR cloning was performed according to the method of Zhu et al., 2007, supra. The homologous ends of the 555 bp PCR product for the first GH61 polypeptide fragment, the homologous ends of the 455 bp PCR product for the second GH61 polypeptide fragment, the homologous ends of the 181 bp PCR product for the third GH61 polypeptide fragment, and plasmid pCW026, digested with Pac I and Pst I, were joined together using an IN-FUSION™ Advantage PCR Cloning Kit. A total of 25 ng of the 555 bp PCR product, 25 ng of the 455 bp PCR product, 25 ng of the 181 bp PCR product, and 200 ng of plasmid pCW026 (digested with Pac I and Pst I) were used in a reaction composed of 2 μl of 5×IN-FUSION™ reaction buffer (Clontech Laboratories, Inc., Mountain View, Calif., USA) and 1 μl of IN-FUSION™ enzyme (Clontech Laboratories, Inc., Mountain View, Calif., USA) in a final volume of 10 μl. The reaction was incubated for 15 minutes at 37° C., followed by 15 minutes at 50° C., and then placed on ice. The reaction volume was increased to 50 μl with 10 mM Tris-0.1 mM EDTA pH 8 (TE) buffer and 3 μl of the reaction was used to transform E. coli XL10-GOLD® Ultracompetent Cells (Stratagene, La Jolla, Calif., USA) according to the manufacturer's instructions. Transformants were selected on LB plates supplemented with 100 μg of ampicillin per ml. Plasmid DNA from several of the resulting E. coli transformants was prepared using a BIOROBOT® 9600.

One plasmid designated pTH226 comprising a polynucleotide (SEQ ID NO: 143) encoding amino acids 1-84 of the T. aurantiacus GH61A polypeptide, amino acids 85-207 from Aspergillus fumigatus GH61B, and amino acids 208-249 of the T. aurantiacus GH61A polypeptide (SEQ ID NO: 144) was identified and the full-length polynucleotide sequence was determined using a 3130×1 Genetic Analyzer (Applied Biosystems, Foster City, Calif., USA).

Example 3 Expression of the Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A Chimeric Polypeptide

Aspergillus oryzae JaL250 (WO 99/61651) protoplasts prepared according to the method of Christensen et al., 1988, supra, were transformed with 5 μg of pTH226 (as well as pAllo2 as a control). The transformation yielded about 20-25 transformants. The transformants were spore purified on PDA plates and then grown in 24-well culture plates composed of 1 ml of either YPG medium or YPM medium and incubated at 34° C. stationary for 5 days. Broth samples were harvested at day 5 and analyzed by SDS-PAGE using a 8-16% Tris-glycine gel (Bio-Rad Laboratories, Inc., Hercules, Calif., USA). Once the cultures from each spore purified transformant were confluent and had sporulated, spore stocks were made by applying 5 ml of sterile filtered 0.01% TWEEN® 80 (diluted with glass distilled water) onto the center of each PDA plate and using a sterile spreader to scrape the spores into solution. Spore stocks from the highest producing transformants identified by SDS-PAGE as having darker bands at the predicted molecular weight of 25 kDa were used to inoculate a 2 liter shake flask containing 300 ml of MDU2BP medium. Shake flasks were incubated for 5 days at 34° C. with agitation at 220 rpm. After the incubation, the broths were sterile filtered using a 0.22 μm polyethersulfone membrane (Millipore, Bedford, Mass., USA) for purification. The A. oryzae strain identified from SDS-PAGE analysis of shake flask broths with the darkest band at 25 kDa was designated A. oryzae TH176.

Example 4 Purification of the Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A Chimeric Polypeptide

The filtered broth of A. oryzae TH176 was first concentrated by a tangential flow concentrator (Pall Filtron, Northborough, Mass., USA) equipped with a 10 kDa polyethersulfone membrane (Pall Filtron, Northborough, Mass., USA), buffer exchanged into 20 mM Tris-HCl pH 8.0, and then purified using a 5 ml Q SEPHAROSE® Fast Flow column (GE Healthcare, Piscataway, N.J., USA) with a 0-600 mM NaCl linear gradient in 20 mM Tris-HCl pH 8.0. Fractions were collected and pooled based on SDS-PAGE. Protein concentration was determined using a Microplate BCA™ Protein Assay Kit in which bovine serum albumin was used as a protein standard.

Example 5 Preparation of Aspergillus fumigatus Beta-Glucosidase

The A. fumigatus beta-glucosidase (SEQ ID NO: 53 [DNA sequence] and SEQ ID NO: 54 [deduced amino acid sequence]) was prepared according to U.S. Pat. No. 7,244,605. Protein concentration was determined using a Microplate BCA™ Protein Assay Kit in which bovine serum albumin was used as a protein standard.

Example 6 Preparation of Phosphoric Acid Swollen Cellulose

Phosphoric acid swollen cellulose (PASC) was prepared from AVICEL® PH101 (FMC, Philadelphia, Pa., USA) using the protocol described by Zhang et al., 2006, Biomacromolecules 7: 644-648.

Example 7 Phosphoric Acid Swollen Cellulose (PASC) Hydrolysis Assay

A 1.0% slurry of PASC prepared as described in Example 6 was thoroughly resuspended by shaking, and quickly transferred to a 100 ml beaker and stirred rapidly with a magnetic stirrer. Five hundred μl aliquots of the 1.0% PASC slurry were pipetted into wells of a 2.0 ml 96-deepwell plate (Axygen, Union City, Calif., USA) using a 1000 μl micropipette with a wide aperture tip (end of tip cut off about 2 mm from the base). One hundred μl of 10 mM MnSO₄-500 mM sodium acetate pH 5 and 100 μl of deionized water were then added to each well. Two hundred μl of either deionized water or a 1.0% pyrogallol (w/w) (Sigma Chemical Co., Inc., St. Louis, Mo., USA) solution was added to each well. Enzyme mixtures were prepared and then added simultaneously to all wells in a volume of 100 μl, for a total of 1 ml in each reaction. The plate was then sealed using an ALPS 300™ plate heat sealer (Abgene, Epsom, United Kingdom), mixed thoroughly, and incubated at either 50° C., 65° C., or 65° C. for approximately 3 days. All experiments were performed in triplicate.

Primary analysis of the hydrolysis reactions was performed using an AGILENT® 1100 HPLC (Agilent Technologies, Inc., Santa Clara, Calif., USA) with CHEMSTATION® software (Agilent Technologies, Inc., Santa Clara, Calif., USA) equipped with an AMINEX™ HPX-87H column (Bio-Rad Laboratories, Inc., Hercules, Calif., USA). After approximately 4 days, the deep-well plate was removed from the incubator and chilled overnight to 4° C. The plate was then mixed well by inversion and briefly centrifuged at 52×g in a SORVALL® RT7 centrifuge (Thermo Fisher Scientific, Aslthan, Mass., USA) for 10 seconds. Samples were then mixed by pipetting, and 200 μl from each well were transferred to a MULTISCREEN® HV centrifuge filter plate assembly (Millipore, Bedford, Mass., USA). The centrifuge filter plate assembly was centrifuged at 2000 rpm in a SORVALL® RT7 centrifuge for 20 minutes. The filtrates were transferred to a 96-well autosampler plate and diluted 1:1 with 5 mM H₂SO₄, sealed with a silicon sealing mat, and inserted into an HPLC injector module (set to 4° C.) for injection of 20 μl onto a CATION H™ guard column connected to a 4.6×250 mm AMINEX® HPX-87H column followed by elution with 0.05% w/w benzoic acid in 5 mM H₂SO₄. Sugars were detected by refractive index detection with quantification by integration compared to purified sugar standards.

All HPLC data processing was performed using MICROSOFT EXCEL™ software (Microsoft, Richland, Wash., USA). Measured glucose concentrations were adjusted for the appropriate dilution factor. Only glucose was measured since beta-glucosidase was at high levels in all samples but the controls. Percent relative conversion was calculated using the following Equation:

% conversion=[sample glucose concentration]/[glucose concentration in a limit digest]×100

In order to calculate % conversion, a 100% conversion point was set based on a cellulase control of 100 mg of Trichoderma reesei cellulase per gram cellulose (CELLUCLAST PLUS™, Novozymes A/S, Bagsvaerd, Denmark), and all values were divided by this number and then multiplied by 100. Triplicate data points were averaged and standard deviation was calculated.

Example 8 Effect of the Addition of the Aspergillus fumigatus GH61B and Thermoascus Aurantiacus GH61A Chimeric Polypeptide on Conversion of Phosphoric Acid Swollen Cellulose by Aspergillus fumigatus Beta-Glucosidase

The A. fumigatus GH61B wild-type polypeptide and the A. fumigatus GH61B and T. aurantiacus GH61A chimeric polypeptide (hereinafter “A. fumigatus GH61B chimeric polypeptide”) were evaluated for their ability to enhance the hydrolysis of phosphoric acid swollen cellulose by A. fumigatus CEL3A beta-glucosidase in the presence of pyrogallol. The phosphoric acid swollen cellulose hydrolysis assay was performed as described in Example 7.

The conversion of phosphoric acid swollen cellulose (0.5% w/w) by the A. fumigatus CEL3A beta-glucosidase (5 mg protein per g cellulose); the combination of the A. fumigatus GH61B wild-type polypeptide (20 mg protein per g cellulose) and the A. fumigatus CEL3A beta-glucosidase (5 mg protein per g cellulose); the combination of the A. fumigatus GH61B chimeric polypeptide (20 mg protein per g cellulose) and the A. fumigatus CEL3A beta-glucosidase (5 mg protein per g cellulose); the combination of pyrogallol (0.2% w/w) and the A. fumigatus CEL3A beta-glucosidase (5 mg protein per g cellulose); the combination of (0.2% w/w) pyrogallol, the A. fumigatus GH61B wild-type polypeptide (20 mg protein per g cellulose), and the A. fumigatus CEL3A beta-glucosidase (5 mg protein per g cellulose); and the combination of pyrogallol (0.2% w/w), the A. fumigatus GH61B chimeric polypeptide (20 mg protein per g cellulose), and the A. fumigatus CEL3A beta-glucosidase (5 mg protein per g cellulose) were assayed as described in Example 7. Data were collected and analyzed, as described in Example 7, after 72 hours of incubation at 50° C., 55° C., and 65° C. The results are shown in FIG. 1.

The A. fumigatus CEL3A beta-glucosidase (5 mg protein per g cellulose) resulted in the conversion of phosphoric acid swollen cellulose of 2.2±0.1% at 50° C. The combination of the A. fumigatus GH61B wild-type polypeptide (20 mg protein per g cellulose) and the A. fumigatus CEL3A beta-glucosidase (5 mg protein per g cellulose) resulted in the conversion of phosphoric acid swollen cellulose of 2.6±0.1% at 50° C. The combination of the A. fumigatus GH61B chimeric polypeptide (20 mg protein per g cellulose) and the A. fumigatus CEL3A beta-glucosidase (5 mg protein per g cellulose) resulted in the conversion of phosphoric acid swollen cellulose of 2.2±0.1% at 50° C. The combination of pyrogallol (0.2% w/w) and the A. fumigatus CEL3A beta-glucosidase (5 mg protein per g cellulose) resulted in the conversion of phosphoric acid swollen cellulose of 2.3±0.1%, 1.6±0.5%, and 1.4±1.1% at 50° C., 60° C. and 65° C., respectively. Addition of the A. fumigatus GH61B wild-type polypeptide (20 mg protein per g cellulose) to the combination of pyrogallol (0.2% w/w) and the A. fumigatus CEL3A beta-glucosidase (5 mg protein per g cellulose) resulted in the conversion of phosphoric acid swollen cellulose of 27.2±0.4%, 17.7±1.2%, and 17.8±0.9% at 50° C., 60° C. and 65° C., respectively.

Addition of the A. fumigatus GH61B chimeric polypeptide (20 mg protein per g cellulose) to the combination of pyrogallol (0.2% w/w) and the A. fumigatus CEL3A beta-glucosidase (5 mg protein per g cellulose) resulted in the conversion of phosphoric acid swollen cellulose of 33.3±1.7%, 24.0±0.3%, and 25.1±0.9% at 50° C., 60° C. and 65° C., respectively.

Example 9 Determination of Td (Denaturation Temperature) of the Aspergillus fumigatus Wild-Type GH61B Polypeptide and the Aspergillus fumigatus GH61B and Thermoascus Aurantiacus GH61A Chimeric Polypeptide by Differential Scanning Calorimetry

The thermostabilities of the A. fumigatus wild-type GH61B polypeptide and the Aspergillus fumigatus GH61B chimeric polypeptide were determined by Differential Scanning calorimetry (DSC) using a VP-Capillary Differential Scanning calorimeter with autosampler (MicroCal Inc., GE Health Care, Piscataway, N.J., USA). The thermal denaturation temperature, Td (° C.), was taken as the top of denaturation peak (major endothermic peak) in thermograms (Cp vs. T) obtained after heating the enzyme solutions in 50 mM sodium acetate pH 5.0 with 100 ppm TRITON® X100 added at a constant programmed heating rate. Approximately 0.4 ml of sample and reference-solutions were stored at 10° C. prior to loading of samples into the calorimeter. Sample and reference (reference: buffer without enzyme) solutions were automatically loaded into the DSC and thermally pre-equilibrated for 20 minutes at 20° C. before the DSC scan was performed from 20° C. to 90° C. at a scan rate of 200 K/hr. Denaturation temperatures were determined at an accuracy of approximately +/−1° C. The results are shown in FIGS. 2A and 2B.

By differential scanning calorimetry, the A. fumigatus wild-type GH61B polypeptide has a Td of approximately 68° C. at pH 5 (FIG. 2A), while the Aspergillus fumigatus GH61B chimeric polypeptide has a Td of approximately 73° C. at pH 5 (FIG. 2B).

Example 10 Preparation of Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A Chimeric Polypeptide Having Cellulolytic Enhancing Activity for Expression in Trichoderma reesei

Plasmid pTH253 was constructed to comprise the Trichoderma reesei cellobiohydrolase I gene promoter and terminator and the Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A chimeric GH61 coding sequence. Two synthetic oligonucleotide primers shown below were designed to PCR amplify the Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A chimeric polypeptide having cellulolytic enhancing activity from plasmid pTH226 and introduce flanking regions for insertion into expression vector pMJ09 (WO 2005/056772). Bold letters represent coding sequence and the remaining sequence is homologous to the insertion sites of pMJ09.

Forward Primer 0610240: (SEQ ID NO: 145) 5′-TCAACCGCGGACTGCGCACCATGTCCTTTTCCAAGATAATTGCT-3′ Reverse Primer 0610241: (SEQ ID NO: 146) 5′-TCGCCACGGAGCTTATTAACCAGTATACAGAGGAGGACC-3′

A total of 50 picomoles of each of the primers above were used in an amplification reaction containing 100 ng of pTH226, 1× PHUSION® Buffer (New England Biolabs, Ipswich, Mass., USA), a 5 μl of a blend of dATP, dTTP, dGTP, and dCTP, each at 10 mM, 1 unit of PHUSION® Taq DNA polymerase (New England Biolabs, Ipswich, Mass., USA) in a final volume of 50 μl. The amplification reaction was performed in an EPPENDORF® MASTERCYCLER® 5333 programmed for 1 cycle at 98° C. for 30 seconds; and 30 cycles each at 98° C. for 10 seconds, 55° C. for 30 seconds, and 72° C. for 1 minute. After the 30 cycles, the reaction was heated for 7 minutes at 72° C. The heat block then went to a 10° C. soak cycle.

The reaction products were isolated by 1.0% agarose gel electrophoresis using TAE buffer where an 890 bp product band was excised from the gel and purified using a QIAQUICK® Gel Extraction Kit according to the manufacturer's instructions.

The 890 bp fragment was then cloned into pMJ09 using an IN-FUSION® Cloning Kit. The vector was digested with Nco I and Pac I and purified by agarose gel electrophoresis as described above. The gene fragment and the digested vector were ligated together in a recombination reaction resulting in the expression plasmid pTH253 in which transcription of the Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A chimeric polypeptide coding sequence were under the control of the T. reesei cbh1 gene promoter. The recombination reaction (20 μl) was composed of 1×IN-FUSION® Buffer (BD Biosciences, Palo Alto, Calif., USA), 1×BSA (BD Biosciences, Palo Alto, Calif., USA), 1 μl of IN-FUSION® enzyme (diluted 1:10) (BD Biosciences, Palo Alto, Calif., USA), 150 ng of pMJ09 digested with Nco I and Pac I, and 60 ng of the Aspergillus fumigatus GH61B or Thermoascus aurantiacus GH61A chimeric polypeptide purified PCR product. The reaction was incubated at 37° C. for 15 minutes followed by 15 minutes at 50° C. The reaction was diluted with 40 μl of 10 mM Tris-0.1 M EDTA buffer and 3 μl of the diluted reaction were used to transform E. coli XL10 SOLOPACK® Gold competent cells according to the manufacturer's instructions. Transformants were selected on LB plates supplemented with 100 μg of ampicillin per ml. Plasmid DNA from several of the resulting E. coli transformants was prepared using a BIOROBOT® 9600.

One plasmid designated pTH253 comprising a polynucleotide (SEQ ID NO: 143) encoding amino acids 1-84 of the T. aurantiacus GH61A polypeptide, amino acids 85-207 from Aspergillus fumigatus GH61B, and amino acids 208-249 of the T. aurantiacus GH61A polypeptide (SEQ ID NO: 144) was identified and the full-length polynucleotide sequence was determined using a 3130×1 Genetic Analyzer.

Example 11 Expression of the Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A Chimeric Polypeptide in Trichoderma reesei

Transformation was utilized to introduce pTH253 encoding the Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A chimeric polypeptide into Trichoderma reesei 981-O-8 (D4) (a mutagenized strain of Trichoderma reesei RutC30; Montenecourt and Eveleigh, 1979, Adv. Chem. Ser. 181: 289-301) by PEG-mediated transformation (Penttila et al., 1987, Gene 61 155-164) to generate T. reesei strain TH178. Each plasmid contained the Aspergillus nidulans amdS gene to enable transformants to grow on acetamide as the sole nitrogen source.

Trichoderma reesei 981-O-8 (D4) was cultivated at 27° C. and 90 rpm in 25 ml of YP medium supplemented with 2% (w/v) glucose and 10 mM uridine for 17 hours. Mycelia were collected by filtration using a Vacuum Driven Disposable Filtration System (Millipore, Bedford, Mass., USA) and washed twice with deionized water and twice with 1.2 M sorbitol. Protoplasts were generated by suspending the washed mycelia in 20 ml of 1.2 M sorbitol containing 15 mg of GLUCANEX™ (Novozymes A/S, Bagsvrd, Denmark) per ml and 0.36 units of chitinase (Sigma Chemical Co., St. Louis, Mo., USA) per ml and incubating for 15-25 minutes at 34° C. with gentle shaking at 90 rpm. Protoplasts were collected by centrifuging for 7 minutes at 400×g and washed twice with cold 1.2 M sorbitol. The protoplasts were counted using a haemacytometer and re-suspended in STC to a final concentration of 1×10⁸ protoplasts per ml. Excess protoplasts were stored in a Cryo 1° C. Freezing Container (Nalgene, Rochester, N.Y., USA) at −80° C.

Approximately 1.2 μg of plasmid pTH253 was digested with Pme I and added to 100 μl of protoplast solution and mixed gently, followed by 250 μl of PEG buffer, mixed, and incubated at room temperature for 30 minutes. STC (3 ml) was then added and mixed and the transformation solution was plated onto COVE plates using Aspergillus nidulans amdS selection. The plates were incubated at 28° C. for 5-7 days. Transformants were sub-cultured onto COVE2 plates and grown at 28° C.

Nineteen transformants were subcultured onto fresh plates containing acetamide and allowed to sporulate for 7 days at 28° C.

The Trichoderma reesei transformants were cultivated in 125 ml baffled shake flasks containing 25 ml of cellulase-inducing medium at pH 6.0 inoculated with spores of the transformants and incubated at 28° C. and 200 rpm for 5 days. Trichoderma reesei 981-O-8 (D4) was run as a control. Culture broth samples were removed at day 5. One ml of each culture broth was centrifuged at 15,700×g for 5 minutes in a micro-centrifuge and the supernatants transferred to new tubes.

SDS-PAGE was carried out using CRITERION® Tris-HCl (5% resolving) gels (Bio-Rad Laboratories, Inc.) with The CRITERION® System (Bio-Rad Laboratories, Inc., Hercules, Calif., USA). Five μl of day 5 supernatants (see above) were suspended in 2× concentration of Laemmli Sample Buffer (Bio-Rad Laboratories, Inc., Hercules, Calif., USA) and boiled in the presence of 5% beta-mercaptoethanol for 5 minutes. The supernatant samples were loaded onto a polyacrylamide gel and subjected to electrophoresis with 1×Tris/Glycine/SDS as running buffer (Bio-Rad Laboratories, Inc., Hercules, Calif., USA). The resulting gel was stained with Bio-Safe Coomassie Stain (Bio-Rad Laboratories, Inc., Hercules, Calif., USA). The transformant showing the highest expression of the Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A chimeric GH61 polypeptide based on the protein gel was designated T. reesei TH178.

Trichoderma reesei TH178 was cultivated in 20-125 ml baffled shake flasks containing 25 ml each of cellulase-inducing medium at pH 6.0. Shake flasks were incubated at 28° C. at 200 rpm for five days. Analysis of the shake flask broths by SDS-PAGE demonstrated expression of a new band, in addition to background Trichoderma reesei proteins, at 25 kDa corresponding to the expected size of the Aspergillus fumigatus GH61B and Thermoascus aurantiacus GH61A chimeric GH61 polypeptide.

The present invention is further described by the following numbered paragraphs:

[1] An isolated chimeric GH61 polypeptide having cellulolytic enhancing activity, comprising: (a) a first GH61 polypeptide fragment at the N-terminal end of the chimeric GH61 polypeptide selected from the group consisting of (i) a polypeptide fragment having at least 60% sequence identity to amino acids 22 to 84 of SEQ ID NO: 78; (ii) a polypeptide fragment encoded by a polynucleotide that hybridizes under at least low stringency conditions with nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polypeptide fragment encoded by a polynucleotide having at least 60% sequence identity to nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof; and (iv) a polypeptide fragment comprising or consisting of amino acids 22 to 84 of SEQ ID NO: 78; (b) a second GH61 polypeptide fragment at the C-terminal end of the first GH61 polypeptide fragment selected from the group consisting of (i) a polypeptide fragment having at least 60% sequence identity to amino acids 85 to 207 of SEQ ID NO: 94; (ii) a polypeptide fragment encoded by a polynucleotide that hybridizes under at least low stringency conditions with nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polypeptide fragment encoded by a polynucleotide having at least 60% sequence identity to nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof; and (iv) a polypeptide fragment comprising or consisting of amino acids 85 to 207 of SEQ ID NO: 94; and (c) a third GH61 polypeptide fragment at the C-terminal end of the second GH61 polypeptide fragment selected from the group consisting of (i) a polypeptide fragment having at least 60% sequence identity to amino acids 208 to 249 of SEQ ID NO: 78; (ii) a polypeptide fragment encoded by a polynucleotide that hybridizes under at least low stringency conditions with nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polypeptide fragment encoded by a polynucleotide having at least 60% sequence identity to nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof; and (iv) a polypeptide fragment comprising or consisting of amino acids 208 to 249 of SEQ ID NO: 78.

[2] The chimeric GH61 polypeptide of paragraph 1, wherein the first GH61 polypeptide fragment has at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100% sequence identity to amino acids 22 to 84 of SEQ ID NO: 78.

[3] The chimeric GH61 polypeptide of paragraph 1, wherein the first GH61 polypeptide fragment is encoded by a polynucleotide that hybridizes under low stringency conditions, medium stringency conditions, medium-high stringency conditions, high stringency conditions, or very high stringency conditions with nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof, or the full-length complement thereof.

[4] The chimeric GH61 polypeptide of paragraph 1, wherein the first GH61 polypeptide fragment is encoded by a polynucleotide having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100% sequence identity to nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof.

[5] The chimeric GH61 polypeptide of paragraph 1, wherein the first GH61 polypeptide fragment comprises or consists of amino acids 22 to 84 of SEQ ID NO: 78.

[6] The chimeric GH61 polypeptide of paragraph 1, wherein the first GH61 polypeptide fragment is encoded by nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof.

[7] The chimeric GH61 polypeptide of paragraph 1, wherein the second GH61 polypeptide fragment has at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100% sequence identity to amino acids 85 to 207 of SEQ ID NO: 94.

[8] The chimeric GH61 polypeptide of paragraph 1, wherein the second GH61 polypeptide fragment is encoded by a polynucleotide that hybridizes under low stringency conditions, medium stringency conditions, medium-high stringency conditions, high stringency conditions, or very high stringency conditions with nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof, or the full-length complement thereof.

[9] The chimeric GH61 polypeptide of paragraph 1, wherein the second GH61 polypeptide fragment is encoded by a polynucleotide having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100% sequence identity to nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof.

[10] The chimeric GH61 polypeptide of paragraph 1, wherein the second GH61 polypeptide fragment comprises or consists of amino acids 85 to 207 of SEQ ID NO: 94.

[11] The chimeric GH61 polypeptide of paragraph 1, wherein the second GH61 polypeptide fragment is encoded by nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof.

[12] The chimeric GH61 polypeptide of paragraph 1, wherein the third GH61 polypeptide fragment has at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100% sequence identity to amino acids 208 to 249 of SEQ ID NO: 78.

[13] The chimeric GH61 polypeptide of paragraph 1, wherein the third GH61 polypeptide fragment is encoded by a polynucleotide that hybridizes under low stringency conditions, medium stringency conditions, medium-high stringency conditions, high stringency conditions, or very high stringency conditions with nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof, or the full-length complement thereof.

[14] The chimeric GH61 polypeptide of paragraph 1, wherein the third GH61 polypeptide fragment is encoded by a polynucleotide having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100% sequence identity to nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof.

[15] The chimeric GH61 polypeptide of paragraph 1, wherein the third GH61 polypeptide fragment comprises or consists of amino acids 208 to 249 of SEQ ID NO: 78.

[16] The chimeric GH61 polypeptide of paragraph 1, wherein the third GH61 polypeptide fragment is encoded by nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof.

[17] The chimeric GH61 polypeptide of paragraph 1, which comprises or consists of amino acids 22 to 84 of SEQ ID NO: 78 as the first GH61 polypeptide fragment at the N-terminal end of the chimeric GH61 polypeptide, amino acids 85 to 207 of SEQ ID NO: 94 as the second GH61 polypeptide fragment at the C-terminal end of the first GH61 polypeptide fragment, and amino acids 208 to 249 of SEQ ID NO: 78 as the third GH61 polypeptide fragment at the C-terminal end of the second GH61 polypeptide fragment.

[18] The chimeric GH61 polypeptide of paragraph 1, which comprises or consists of the mature polypeptide of SEQ ID NO: 144.

[19] The chimeric GH61 polypeptide of any of paragraphs 1-18, which further comprises a signal peptide at the N-terminal end of the first GH61 polypeptide fragment.

[20] The chimeric GH61 polypeptide of paragraph 19, wherein the signal peptide is the signal peptide of SEQ ID NO: 78.

[21] The chimeric GH61 polypeptide of paragraph 19, wherein the signal peptide is amino acids 1 to 21 of SEQ ID NO: 78.

[22] An isolated polynucleotide encoding the chimeric GH61 polypeptide of any of paragraphs 1-21.

[23] A nucleic acid construct comprising the polynucleotide of paragraph 22.

[24] An expression vector comprising the polynucleotide of paragraph 22.

[25] A host cell comprising the polynucleotide of paragraph 22.

[26] A method of producing a chimeric GH61 polypeptide having cellulolytic enhancing activity, comprising: (a) cultivating the host cell of paragraph 25 under conditions suitable for the expression of the chimeric GH61 polypeptide; and (b) recovering the chimeric GH61 polypeptide.

[27] A transgenic plant, plant part or plant cell transformed with the polynucleotide of paragraph 20 encoding a chimeric GH61 polypeptide.

[28] A method of producing the chimeric GH61 polypeptide of any of paragraphs 1-21, comprising: (a) cultivating a transgenic plant or a plant cell comprising a polynucleotide encoding the chimeric GH61 polypeptide under conditions conducive for production of the chimeric GH61 polypeptide; and (b) recovering the chimeric GH61 polypeptide.

[29] A method for degrading or converting a cellulosic material, comprising: treating the cellulosic material with an enzyme composition in the presence of the chimeric GH61 polypeptide of any of paragraphs 1-21.

[30] The method of paragraph 29, wherein the cellulosic material is pretreated.

[31] The method of paragraph 29 or 30, further comprising recovering the degraded cellulosic material.

[32] The method of any of paragraphs 29-31, wherein the enzyme composition comprises one or more enzymes selected from the group consisting of a cellulase, a hemicellulase, an esterase, an expansin, a laccase, a ligninolytic enzyme, a pectinase, a peroxidase, a protease, and a swollenin.

[33] The method of paragraph 32, wherein the cellulase is one or more enzymes selected from the group consisting of an endoglucanase, a cellobiohydrolase, and a beta-glucosidase.

[34] The method of paragraph 32, wherein the hemicellulase is one or more enzymes selected from the group consisting of a xylanase, an acetyxylan esterase, a feruloyl esterase, an arabinofuranosidase, a xylosidase, and a glucuronidase.

[35] The method of any of paragraphs 29-34, wherein the degraded cellulosic material is a sugar.

[36] The method of paragraph 35, wherein the sugar is selected from the group consisting of glucose, xylose, mannose, galactose, and arabinose.

[37] A method for producing a fermentation product, comprising: (a) saccharifying a cellulosic material with an enzyme composition in the presence of the chimeric GH61 polypeptide of any of paragraphs 1-21; (b) fermenting the saccharified cellulosic material with one or more fermenting microorganisms to produce the fermentation product; and (c) recovering the fermentation product from the fermentation.

[38] The method of paragraph 37, wherein the cellulosic material is pretreated.

[39] The method of paragraph 37 or 38, wherein the enzyme composition comprises one or more enzymes selected from the group consisting of a cellulase, a hemicellulase, an esterase, an expansin, a laccase, a ligninolytic enzyme, a pectinase, a peroxidase, a protease, and a swollenin.

[40] The method of paragraph 39, wherein the cellulase is one or more enzymes selected from the group consisting of an endoglucanase, a cellobiohydrolase, and a beta-glucosidase.

[41] The method of paragraph 39, wherein the hemicellulase is one or more enzymes selected from the group consisting of a xylanase, an acetyxylan esterase, a feruloyl esterase, an arabinofuranosidase, a xylosidase, and a glucuronidase.

[42] The method of any of paragraphs 37-41, wherein steps (a) and (b) are performed simultaneously in a simultaneous saccharification and fermentation.

[43] The method of any of paragraphs 37-42, wherein the fermentation product is an alcohol, an alkane, a cycloalkane, an alkene, an amino acid, a gas, isoprene, a ketone, an organic acid, or polyketide.

[44] A method of fermenting a cellulosic material, comprising: fermenting the cellulosic material with one or more fermenting microorganisms, wherein the cellulosic material is saccharified with an enzyme composition in the presence of the chimeric GH61 polypeptide of any of paragraphs 1-21.

[45] The method of paragraph 44, wherein the cellulosic material is pretreated before saccharification.

[46] The method of paragraph 44 or 45, wherein the enzyme composition comprises one or more enzymes selected from the group consisting of a cellulase, a hemicellulase, an esterase, an expansin, a laccase, a ligninolytic enzyme, a pectinase, a peroxidase, a protease, and a swollenin.

[47] The method of paragraph 46, wherein the cellulase is one or more enzymes selected from the group consisting of an endoglucanase, a cellobiohydrolase, and a beta-glucosidase.

[48] The method of paragraph 46, wherein the hemicellulase is one or more enzymes selected from the group consisting of a xylanase, an acetyxylan esterase, a feruloyl esterase, an arabinofuranosidase, a xylosidase, and a glucuronidase.

[49] The method of any of paragraphs 44-48, wherein the fermenting of the cellulosic material produces a fermentation product.

[50] The method of paragraph 49, further comprising recovering the fermentation product from the fermentation.

[51] The method of any of paragraphs 49 or 50, wherein the fermentation product is an alcohol, an alkane, a cycloalkane, an alkene, an amino acid, a gas, isoprene, a ketone, an organic acid, or polyketide.

[52] Use of the chimeric GH61 polypeptide of any of paragraphs 1-21 in detergents.

[53] A detergent composition comprising the chimeric GH61 polypeptide of any of paragraphs 1-21 and a surfactant.

[54] The composition of paragraph 53, further comprising one or more enzymes selected from the group consisting of an amylase, arabinase, cutinase, carbohydrase, cellulase, galactanase, laccase, lipase, mannanase, oxidase, pectinase, peroxidase, protease, and xylanase.

[55] The composition of paragraph 53 or 54, which is formulated as a bar, a tablet, a powder, a granule, a paste, or a liquid.

[56] A method for cleaning or washing a hard surface or laundry, the method comprising contacting the hard surface or the laundry with the composition of any of paragraphs 53-55.

[57] A whole broth formulation or cell culture composition comprising the chimeric GH61 polypeptide of any of paragraps 1-21.

The invention described and claimed herein is not to be limited in scope by the specific aspects herein disclosed, since these aspects are intended as illustrations of several aspects of the invention. Any equivalent aspects are intended to be within the scope of this invention. Indeed, various modifications of the invention in addition to those shown and described herein will become apparent to those skilled in the art from the foregoing description. Such modifications are also intended to fall within the scope of the appended claims. In the case of conflict, the present disclosure including definitions will control. 

1. An isolated chimeric GH61 polypeptide having cellulolytic enhancing activity, comprising: (a) a first GH61 polypeptide fragment at the N-terminal end of the chimeric GH61 polypeptide selected from the group consisting of (i) a polypeptide fragment having at least 60% sequence identity to amino acids 22 to 84 of SEQ ID NO: 78; (ii) a polypeptide fragment encoded by a polynucleotide that hybridizes under at least low stringency conditions with nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polypeptide fragment encoded by a polynucleotide having at least 60% sequence identity to nucleotides 64 to 301 of SEQ ID NO: 77 or the cDNA sequence thereof; and (iv) a polypeptide fragment comprising or consisting of amino acids 22 to 84 of SEQ ID NO: 78; (b) a second GH61 polypeptide fragment at the C-terminal end of the first GH61 polypeptide fragment selected from the group consisting of (i) a polypeptide fragment having at least 60% sequence identity to amino acids 85 to 207 of SEQ ID NO: 94; (ii) a polypeptide fragment encoded by a polynucleotide that hybridizes under at least low stringency conditions with nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polypeptide fragment encoded by a polynucleotide having at least 60% sequence identity to nucleotides 306 to 730 of SEQ ID NO: 93 or the cDNA sequence thereof; and (iv) a polypeptide fragment comprising or consisting of amino acids 85 to 207 of SEQ ID NO: 94; and (c) a third GH61 polypeptide fragment at the C-terminal end of the second GH61 polypeptide fragment selected from the group consisting of (i) a polypeptide fragment having at least 60% sequence identity to amino acids 208 to 249 of SEQ ID NO: 78; (ii) a polypeptide fragment encoded by a polynucleotide that hybridizes under at least low stringency conditions with nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof, or the full-length complement thereof; (iii) a polypeptide fragment encoded by a polynucleotide having at least 60% sequence identity to nucleotides 671 to 796 of SEQ ID NO: 77 or the cDNA sequence thereof; and (iv) a polypeptide fragment comprising or consisting of amino acids 208 to 249 of SEQ ID NO:
 78. 2. The chimeric GH61 polypeptide of claim 1, wherein the first GH61 polypeptide fragment comprises or consists of amino acids 22 to 84 of SEQ ID NO:
 78. 3. The chimeric GH61 polypeptide of claim 1, wherein the second GH61 polypeptide fragment comprises or consists of amino acids 85 to 207 of SEQ ID NO:
 94. 4. The chimeric GH61 polypeptide of claim 1, wherein the third GH61 polypeptide fragment comprises or consists of amino acids 208 to 249 of SEQ ID NO:
 78. 5. The chimeric GH61 polypeptide of claim 1, which comprises or consists of amino acids 22 to 84 of SEQ ID NO: 78 as the first GH61 polypeptide fragment at the N-terminal end of the chimeric GH61 polypeptide, amino acids 85 to 207 of SEQ ID NO: 94 as the second GH61 polypeptide fragment at the C-terminal end of the first GH61 polypeptide fragment, and amino acids 208 to 249 of SEQ ID NO: 78 as the third GH61 polypeptide fragment at the C-terminal end of the second GH61 polypeptide fragment.
 6. The chimeric GH61 polypeptide of claim 1, which comprises or consists of the mature polypeptide of SEQ ID NO:
 144. 7. An isolated polynucleotide encoding the chimeric GH61 polypeptide of claim
 1. 8. A host cell comprising the polynucleotide of claim
 7. 9. A method of producing a chimeric GH61 polypeptide having cellulolytic enhancing activity, comprising: (a) cultivating the host cell of claim 8 under conditions suitable for the expression of the chimeric GH61 polypeptide; and (b) recovering the chimeric GH61 polypeptide.
 10. A transgenic plant, plant part or plant cell transformed with the polynucleotide of claim 7 encoding a chimeric GH61 polypeptide.
 11. A method of producing the chimeric GH61 polypeptide of claim 1, comprising: (a) cultivating a transgenic plant or a plant cell comprising a polynucleotide encoding the chimeric GH61 polypeptide under conditions conducive for production of the chimeric GH61 polypeptide; and (b) recovering the chimeric GH61 polypeptide.
 12. A method for degrading or converting a cellulosic material, comprising: treating the cellulosic material with an enzyme composition in the presence of the chimeric GH61 polypeptide of claim
 1. 13. The method of claim 12, further comprising recovering the degraded cellulosic material.
 14. The method of claim 12, wherein the enzyme composition comprises one or more enzymes selected from the group consisting of a cellulase, a hemicellulase, a polypeptide having cellulolytic enhancing activity, an esterase, an expansin, a laccase, a ligninolytic enzyme, a pectinase, a peroxidase, a protease, and a swollenin.
 15. The method of claim 12, wherein the degraded cellulosic material is a sugar.
 16. A method for producing a fermentation product, comprising: (a) saccharifying a cellulosic material with an enzyme composition in the presence of the chimeric GH61 polypeptide of claim 1; (b) fermenting the saccharified cellulosic material with one or more fermenting microorganisms to produce the fermentation product; and (c) recovering the fermentation product from the fermentation.
 17. The method of claim 16, wherein the enzyme composition comprises one or more enzymes selected from the group consisting of a cellulase, a hemicellulase, a polypeptide having cellulolytic enhancing activity, an esterase, an expansin, a laccase, a ligninolytic enzyme, a pectinase, a peroxidase, a protease, and a swollenin.
 18. A method of fermenting a cellulosic material, comprising: fermenting the cellulosic material with one or more fermenting microorganisms, wherein the cellulosic material is saccharified with an enzyme composition in the presence of the chimeric GH61 polypeptide of claim
 1. 19. The method of claim 18, wherein the enzyme composition comprises one or more enzymes selected from the group consisting of a cellulase, a hemicellulase, a polypeptide having cellulolytic enhancing activity, an esterase, an expansin, a laccase, a ligninolytic enzyme, a pectinase, a peroxidase, a protease, and a swollenin.
 20. The method of claim 18, wherein the fermenting of the cellulosic material produces a fermentation product.
 21. The method of claim 20, further comprising recovering the fermentation product from the fermentation.
 22. (canceled)
 23. A detergent composition comprising the chimeric GH61 polypeptide of claim 1 and a surfactant.
 24. A method for cleaning or washing a hard surface or laundry, comprising contacting the hard surface or the laundry with the composition of claim
 23. 25. A whole broth formulation or cell culture composition comprising the chimeric GH61 polypeptide of claim
 1. 